A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv847699



Internal ID15794969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85237085..85383609hg38UCSC Ensembl
Innerchr15:85780316..85926840hg19UCSC Ensembl
Innerchr15:83581320..83727844hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38146525
hg19146525
hg18146525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570296
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)nssv847699
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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