A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv847704



Internal ID15794974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85282336..85564521hg38UCSC Ensembl
Innerchr15:85825567..86107752hg19UCSC Ensembl
Innerchr15:83626571..83908756hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38282186
hg19282186
hg18282186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570301
Supporting Variants
Samples
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv847704
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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