A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848956



Internal ID15796226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94237012..94285237hg38UCSC Ensembl
Innerchr15:94780241..94828466hg19UCSC Ensembl
Innerchr15:92581245..92629470hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3848226
hg1948226
hg1848226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570530
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)nssv848956
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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