A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569969



Internal ID16357378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73368274..73376566hg38UCSC Ensembl
Innerchr15:73660615..73668907hg19UCSC Ensembl
Innerchr15:71447668..71455960hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg388293
hg198293
hg188293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845257
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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