A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524806



Internal ID18476401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:89756671..89943559hg38UCSC Ensembl
Innerchr12:90150448..90337336hg19UCSC Ensembl
Innerchr12:88674579..88861467hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38186889
hg19186889
hg18186889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044897
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)nssv3524806
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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