A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570236



Internal ID16357645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81307102..81308232hg38UCSC Ensembl
Innerchr15:81599443..81600573hg19UCSC Ensembl
Innerchr15:79386498..79387628hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381131
hg191131
hg181131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847552
Samples
Known GenesIL16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570236
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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