A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817534



Internal ID16111490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95073612..95078936hg38UCSC Ensembl
Innerchr13:95725866..95731190hg19UCSC Ensembl
Innerchr13:94523867..94529191hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg385325
hg195325
hg185325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562767
Supporting Variants
Samples
Known GenesABCC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817534
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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