A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569156



Internal ID16356565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35394066..35425212hg38UCSC Ensembl
Innerchr15:35686267..35717413hg19UCSC Ensembl
Innerchr15:33473559..33504705hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3831147
hg1931147
hg1831147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840434
Samples
Known GenesDPH6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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