A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569799



Internal ID16010522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67511204..67585107hg38UCSC Ensembl
Innerchr15:67803542..67877445hg19UCSC Ensembl
Innerchr15:65590596..65664499hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3873904
hg1973904
hg1873904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844322
Samples
Known GenesC15orf61, IQCH-AS1, MAP2K5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569799
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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