A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv806780



Internal ID16100736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:25658152..25693380hg38UCSC Ensembl
Innerchr13:26232290..26267518hg19UCSC Ensembl
Innerchr13:25130290..25165518hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3835229
hg1935229
hg1835229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561354
Supporting Variants
Samples
Known GenesATP8A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv806780
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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