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nsv6275619

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:133

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
Submitted genomic64,464,171-64,464,303Question Mark
Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):64,930,889-64,931,021Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6275619Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1464,464,17164,464,303
nsv6275619RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1464,930,88964,931,021

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17924086deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17924086Submitted genomicNC_000014.9:g.6446
4171_64464303del
GRCh38 (hg38)NC_000014.9Chr1464,464,17164,464,303
nssv17924086RemappedPerfectNC_000014.8:g.6493
0889_64931021del
GRCh37.p13First PassNC_000014.8Chr1464,930,88964,931,021

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)
nssv17924086<0.00122318
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