A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv847703



Internal ID15794973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85272357..85600273hg38UCSC Ensembl
Innerchr15:85815588..86143504hg19UCSC Ensembl
Innerchr15:83616592..83944508hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38327917
hg19327917
hg18327917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570300
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)nssv847703
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer