A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv845289



Internal ID16139245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75201482..75245134hg38UCSC Ensembl
Innerchr15:75493823..75537475hg19UCSC Ensembl
Innerchr15:73280876..73324528hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3843653
hg1943653
hg1843653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569995
Supporting Variants
Samples
Known GenesC15orf39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv845289
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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