A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569991



Internal ID16010714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74592750..74655722hg38UCSC Ensembl
Innerchr15:74885091..74948063hg19UCSC Ensembl
Innerchr15:72672144..72735116hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3862973
hg1962973
hg1862973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149603
SamplesNINDS_70
Known GenesARID3B, CLK3, EDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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