A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526164



Internal ID18824445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:128369985..128397661hg38UCSC Ensembl
Innerchr12:128854530..128882206hg19UCSC Ensembl
Innerchr12:127420483..127448159hg18UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3827677
hg1927677
hg1827677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046660
Supporting Variants
Samples
Known GenesTMEM132C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3526164
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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