A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569996



Internal ID16357405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75201482..75248150hg38UCSC Ensembl
Innerchr15:75493823..75540491hg19UCSC Ensembl
Innerchr15:73280876..73327544hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3846669
hg1946669
hg1846669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4627n54
Supporting Variantsnssv845290
Samples
Known GenesC15orf39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569996
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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