nsv471343

  • Variant Calls:3
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:28,278

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 360 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):16,563,917-16,592,194Question Mark
Overlapping variant regions from other studies: 360 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):16,890,412-16,918,689Question Mark
Overlapping variant regions from other studies: 54 SVs from 11 studies. See in: genome view    
Submitted genomic16,635,718-16,663,995Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv471343RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr116,563,91716,592,194
nsv471343RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr116,890,41216,918,689
nsv471343Submitted genomicNCBI35 (hg17)NC_000001.8Chr116,635,71816,663,995

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv548025copy number gainJDWSequencingRead depth49198
nssv548026copy number gainNA18507SequencingRead depth52208
nssv548027copy number gainYHSequencingRead depth49201

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nssv548025RemappedPerfectNC_000001.11:g.(16
563917_?)_(?_16592
194)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr116,563,91716,592,194
nssv548026RemappedPerfectNC_000001.11:g.(16
563917_?)_(?_16592
194)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr116,563,91716,592,194
nssv548027RemappedPerfectNC_000001.11:g.(16
563917_?)_(?_16592
194)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr116,563,91716,592,194
nssv548025RemappedPerfectNC_000001.10:g.(16
890412_?)_(?_16918
689)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr116,890,41216,918,689
nssv548026RemappedPerfectNC_000001.10:g.(16
890412_?)_(?_16918
689)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr116,890,41216,918,689
nssv548027RemappedPerfectNC_000001.10:g.(16
890412_?)_(?_16918
689)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr116,890,41216,918,689
nssv548025Submitted genomicNC_000001.8:g.(166
35718_?)_(?_166639
95)dup
NCBI35 (hg17)NC_000001.8Chr116,635,71816,663,995
nssv548026Submitted genomicNC_000001.8:g.(166
35718_?)_(?_166639
95)dup
NCBI35 (hg17)NC_000001.8Chr116,635,71816,663,995
nssv548027Submitted genomicNC_000001.8:g.(166
35718_?)_(?_166639
95)dup
NCBI35 (hg17)NC_000001.8Chr116,635,71816,663,995

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
nssv5480254JDWOligo aCGHProbe signal intensityPass
nssv5480264NA18507Oligo aCGHProbe signal intensityPass
nssv5480274YHOligo aCGHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant