A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848953



Internal ID15796223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93806223..94205499hg38UCSC Ensembl
Innerchr15:94349452..94748728hg19UCSC Ensembl
Innerchr15:92150456..92549732hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38399277
hg19399277
hg18399277
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570526
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)nssv848953
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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