A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526165



Internal ID18824446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:128570557..128629200hg38UCSC Ensembl
Innerchr12:129055102..129113745hg19UCSC Ensembl
Innerchr12:127621055..127679698hg18UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3858644
hg1958644
hg1858644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047578
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)nssv3526165
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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