A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv847702



Internal ID15794972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85272357..85600205hg38UCSC Ensembl
Innerchr15:85815588..86143436hg19UCSC Ensembl
Innerchr15:83616592..83944440hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38327849
hg19327849
hg18327849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570299
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)nssv847702
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