A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561349



Internal ID16002072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24700388..24755064hg38UCSC Ensembl
Innerchr13:25274526..25329202hg19UCSC Ensembl
Innerchr13:24172526..24227202hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3854677
hg1954677
hg1854677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3093n54
Supporting Variantsnssv806775
Samples
Known GenesATP12A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561349
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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