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nsv6210649

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 26 studies. See in: genome view    
Submitted genomic54,711,547-54,711,600Question Mark
Overlapping variant regions from other studies: 32 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):685,914-685,967Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6210649Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1954,711,54754,711,600
nsv6210649RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004166865.1Chr19|NW_0
04166865.1
685,914685,967

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17947412deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17947412Submitted genomicNC_000019.10:g.547
11547_54711600del
GRCh38 (hg38)NC_000019.10Chr1954,711,54754,711,600
nssv17947412RemappedPerfectNW_004166865.1:g.6
85914_685967del
GRCh37.p13First PassNW_004166865.1Chr19|NW_0
04166865.1
685,914685,967

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)
nssv179474120.00252320
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