A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524900



Internal ID18476495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109348210..109377067hg38UCSC Ensembl
Innerchr12:109786015..109814872hg19UCSC Ensembl
Innerchr12:108270398..108299255hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3828858
hg1928858
hg1828858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039514
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)nssv3524900
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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