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nsv6201964

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:295

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 163 SVs from 47 studies. See in: genome view    
Submitted genomic128,708,116-128,708,410Question Mark
Overlapping variant regions from other studies: 163 SVs from 47 studies. See in: genome view    
Remapped(Score: Perfect):129,192,661-129,192,955Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6201964Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12128,708,116128,708,410
nsv6201964RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12129,192,661129,192,955

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17924397deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17924397Submitted genomicNC_000012.12:g.128
708116_128708410de
l
GRCh38 (hg38)NC_000012.12Chr12128,708,116128,708,410
nssv17924397RemappedPerfectNC_000012.11:g.129
192661_129192955de
l
GRCh37.p13First PassNC_000012.11Chr12129,192,661129,192,955

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)
nssv179243970.0042498
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