A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv819761



Internal ID16113717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110676272..110678007hg38UCSC Ensembl
Innerchr13:111328619..111330354hg19UCSC Ensembl
Innerchr13:110126620..110128355hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381736
hg191736
hg181736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563127
Supporting Variants
Samples
Known GenesCARS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv819761
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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