A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609740



Internal ID16397149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:3610183..3620923hg38UCSC Ensembl
Innerchr8:3467705..3478445hg19UCSC Ensembl
Innerchr8:3455113..3465853hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg3810741
hg1910741
hg1810741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156113
SamplesHGDP00903
Known GenesCSMD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609740
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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