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nsv6144641

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 394 SVs from 54 studies. See in: genome view    
Submitted genomic17,268,000-17,328,000Question Mark
Overlapping variant regions from other studies: 394 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):17,378,809-17,438,809Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6144641Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1917,268,00017,328,000
nsv6144641RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1917,378,80917,438,809

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721931duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721931Submitted genomicNC_000019.10:g.172
68000_17328000dup
GRCh38 (hg38)NC_000019.10Chr1917,268,00017,328,000
nssv17721931RemappedPerfectNC_000019.9:g.1737
8809_17438809dup
GRCh37.p13First PassNC_000019.9Chr1917,378,80917,438,809

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)
nssv177219310.004184068
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