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nsv5503897

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 62 SVs from 19 studies. See in: genome view    
Submitted genomic61,815,230-61,815,282Question Mark
Overlapping variant regions from other studies: 62 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):61,582,702-61,582,754Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5503897Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1161,815,23061,815,282
nsv5503897RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1161,582,70261,582,754

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046582deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046582Submitted genomicNC_000011.10:g.618
15230_61815282del
GRCh38 (hg38)NC_000011.10Chr1161,815,23061,815,282
nssv17046582RemappedPerfectNC_000011.9:g.6158
2702_61582754del
GRCh37.p13First PassNC_000011.9Chr1161,582,70261,582,754

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17046582<0.00136404
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