A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv819762



Internal ID15767032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110676418..110678021hg38UCSC Ensembl
Innerchr13:111328765..111330368hg19UCSC Ensembl
Innerchr13:110126766..110128369hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381604
hg191604
hg181604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563128
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)nssv819762
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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