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nsv5495057

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 900 SVs from 84 studies. See in: genome view    
Submitted genomic4,272,500-4,437,500Question Mark
Overlapping variant regions from other studies: 900 SVs from 84 studies. See in: genome view    
Remapped(Score: Perfect):4,293,730-4,458,730Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5495057Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr114,272,5004,437,500
nsv5495057RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr114,293,7304,458,730

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17041603duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17041603Submitted genomicNC_000011.10:g.427
2500_4437500dup
GRCh38 (hg38)NC_000011.10Chr114,272,5004,437,500
nssv17041603RemappedPerfectNC_000011.9:g.4293
730_4458730dup
GRCh37.p13First PassNC_000011.9Chr114,293,7304,458,730

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)
nssv17041603<0.00156400
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