esv1791972

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,108

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 49 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):34,656,185-34,657,292Question Mark
Overlapping variant regions from other studies: 49 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):34,656,290-34,657,397Question Mark
Overlapping variant regions from other studies: 42 SVs from 8 studies. See in: genome view    
Submitted genomic34,692,047-34,693,154Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv1791972RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000005.10Chr534,656,18534,657,292
esv1791972RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000005.9Chr534,656,29034,657,397
esv1791972Submitted genomicNCBI36 (hg18)NC_000005.8Chr534,692,04734,693,154

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv4397752copy number lossNA12239SNP arraySNP genotyping analysis12,430

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
essv4397752RemappedPerfectNC_000005.10:g.(?_
34656185)_(3465729
2_?)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000005.10Chr534,656,18534,657,292
essv4397752RemappedPerfectNC_000005.9:g.(?_3
4656290)_(34657397
_?)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000005.9Chr534,656,29034,657,397
essv4397752Submitted genomicNC_000005.8:g.(?_3
4692047)_(34693154
_?)del
NCBI36 (hg18)NC_000005.8Chr534,692,04734,693,154

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant