A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv847392



Internal ID16141348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77818933..77819835hg38UCSC Ensembl
Innerchr15:78111275..78112177hg19UCSC Ensembl
Innerchr15:75898330..75899232hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38903
hg19903
hg18903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570180
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)nssv847392
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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