A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149220



Internal ID15529620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25678071..25691886hg38UCSC Ensembl
Innerchr15:25923218..25937033hg19UCSC Ensembl
Innerchr15:23474311..23488126hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3813816
hg1913816
hg1813816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568586
Supporting Variants
SamplesHGDP00819
Known GenesATP10A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149220
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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