A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526801



Internal ID18825082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64683335..64740951hg38UCSC Ensembl
Innerchr13:65257467..65315083hg19UCSC Ensembl
Innerchr13:64155468..64213084hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3857617
hg1957617
hg1857617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044887
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)nssv3526801
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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