A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132737



Internal ID19249482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:65662545..65688645hg38UCSC Ensembl
Outerchr9:70477400..70503500hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3826101
hg1926101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4057n106
Supporting Variantsnssv3987527
SamplesKWS1
Known GenesCBWD3, CBWD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132737
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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