A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612982



Internal ID16400391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95343..156659hg38UCSC Ensembl
Innerchr9:95343..156659hg19UCSC Ensembl
Innerchr9:85343..146659hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3861317
hg1961317
hg1861317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1125841, nssv1125842
Samples
Known GenesCBWD1, FOXD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612982
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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