A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848199



Internal ID15795469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:88806095..88830608hg38UCSC Ensembl
Innerchr15:89349326..89373839hg19UCSC Ensembl
Innerchr15:87150330..87174843hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3824514
hg1924514
hg1824514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570385
Supporting Variants
Samples
Known GenesACAN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv848199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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