A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613731



Internal ID16054454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19400353..19448475hg38UCSC Ensembl
Innerchr9:19400351..19448473hg19UCSC Ensembl
Innerchr9:19390351..19438473hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3848123
hg1948123
hg1848123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130784
Samples
Known GenesACER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613731
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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