A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569968



Internal ID16357377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73368274..73372400hg38UCSC Ensembl
Innerchr15:73660615..73664741hg19UCSC Ensembl
Innerchr15:71447668..71451794hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg384127
hg194127
hg184127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845256
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569968
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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