A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712452



Internal ID19010733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:38514440..38601984hg38UCSC Ensembl
Innerchr12:38908242..38995786hg19UCSC Ensembl
Innerchr12:37194509..37282053hg18UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3887545
hg1987545
hg1887545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040304
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712452
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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