A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570298



Internal ID16011021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85272357..85510128hg38UCSC Ensembl
Innerchr15:85815588..86053359hg19UCSC Ensembl
Innerchr15:83616592..83854363hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38237772
hg19237772
hg18237772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847701
Samples
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570298
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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