A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505068



Internal ID18456663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:18208543..18260193hg38UCSC Ensembl
Innerchr12:18361477..18413127hg19UCSC Ensembl
Innerchr12:18252744..18304394hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3851651
hg1951651
hg1851651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037527
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)nssv3505068
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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