A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987527



Internal ID19212635
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 StatusS
Merged Variantsnsv1132737
Supporting Variants
SamplesKWS1
Known GenesCBWD3, CBWD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987527
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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