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nsv5501642

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 270 SVs from 52 studies. See in: genome view    
Submitted genomic9,416,512-9,431,512Question Mark
Overlapping variant regions from other studies: 270 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):9,569,108-9,584,108Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5501642Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,416,5129,431,512
nsv5501642RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr129,569,1089,584,108

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052804deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052804Submitted genomicNC_000012.12:g.941
6512_9431512del
GRCh38 (hg38)NC_000012.12Chr129,416,5129,431,512
nssv17052804RemappedPerfectNC_000012.11:g.956
9108_9584108del
GRCh37.p13First PassNC_000012.11Chr129,569,1089,584,108

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)
nssv17052804<0.00126276
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