A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149255



Internal ID15508969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85282336..85600273hg38UCSC Ensembl
Innerchr15:85825567..86143504hg19UCSC Ensembl
Innerchr15:83626571..83944508hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38317938
hg19317938
hg18317938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570303
Supporting Variants
Samples1782681216_A
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149255
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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