A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562767



Internal ID16350176
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 StatusM
Merged Variants
Supporting Variantsnssv817534
Samples
Known GenesABCC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562767
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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