A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv806776



Internal ID15754046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24700388..24756889hg38UCSC Ensembl
Innerchr13:25274526..25331027hg19UCSC Ensembl
Innerchr13:24172526..24229027hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3856502
hg1956502
hg1856502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561350
Supporting Variants
Samples
Known GenesATP12A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv806776
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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