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nsv5503518

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:282

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 93 SVs from 24 studies. See in: genome view    
Submitted genomic107,772,422-107,772,703Question Mark
Overlapping variant regions from other studies: 93 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):108,166,199-108,166,480Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5503518Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12107,772,422107,772,703
nsv5503518RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12108,166,199108,166,480

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684268deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684268Submitted genomicNC_000012.12:g.107
772422_107772703de
l
GRCh38 (hg38)NC_000012.12Chr12107,772,422107,772,703
nssv17684268RemappedPerfectNC_000012.11:g.108
166199_108166480de
l
GRCh37.p13First PassNC_000012.11Chr12108,166,199108,166,480

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)
nssv176842680.00176404
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