A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv850620



Internal ID16144576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99433164..99446559hg38UCSC Ensembl
Innerchr15:99973369..99986764hg19UCSC Ensembl
Innerchr15:97790892..97804287hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3813396
hg1913396
hg1813396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570728
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv850620
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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