A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523216



Internal ID18821497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:27190174..27237161hg38UCSC Ensembl
Innerchr13:27764311..27811298hg19UCSC Ensembl
Innerchr13:26662311..26709298hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3846988
hg1946988
hg1846988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054632
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)nssv3523216
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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