A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147212



Internal ID19195382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:65662745..65681046hg38UCSC Ensembl
Outerchr9:70484999..70503300hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3818302
hg1918302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999989
SamplesKWB1
Known GenesCBWD3, CBWD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147212
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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