nsv821607

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,744

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 252 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):92,935,864-92,938,607Question Mark
Overlapping variant regions from other studies: 252 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):93,857,015-93,859,758Question Mark
Overlapping variant regions from other studies: 176 SVs from 18 studies. See in: genome view    
Submitted genomic94,076,038-94,078,781Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv821607RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000004.12Chr492,935,86492,938,607
nsv821607RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000004.11Chr493,857,01593,859,758
nsv821607Submitted genomicNCBI36 (hg18)NC_000004.10Chr494,076,03894,078,781

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1420430deletionNA10851SequencingRead depth1,299

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv1420430RemappedPerfectNC_000004.12:g.(?_
92935864)_(9293860
7_?)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000004.12Chr492,935,86492,938,607
nssv1420430RemappedPerfectNC_000004.11:g.(?_
93857015)_(9385975
8_?)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000004.11Chr493,857,01593,859,758
nssv1420430Submitted genomicNC_000004.10:g.(?_
94076038)_(9407878
1_?)del
NCBI36 (hg18)NC_000004.10Chr494,076,03894,078,781

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

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