A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149164



Internal ID15875442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97536805..97599419hg38UCSC Ensembl
Innerchr15:98080035..98142649hg19UCSC Ensembl
Innerchr15:95881039..95943653hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3862615
hg1962615
hg1862615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570639
Supporting Variants
SamplesHGDP00684
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149164
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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