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nsv5500677

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,552

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 109 SVs from 33 studies. See in: genome view    
Submitted genomic118,056,707-118,060,258Question Mark
Overlapping variant regions from other studies: 109 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):118,494,512-118,498,063Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5500677Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12118,056,707118,060,258
nsv5500677RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12118,494,512118,498,063

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684779deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684779Submitted genomicNC_000012.12:g.118
056707_118060258de
l
GRCh38 (hg38)NC_000012.12Chr12118,056,707118,060,258
nssv17684779RemappedPerfectNC_000012.11:g.118
494512_118498063de
l
GRCh37.p13First PassNC_000012.11Chr12118,494,512118,498,063

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)
nssv17684779<0.00126404
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