A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959689



Internal ID18873271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:11300..35500hg38UCSC Ensembl
Outerchr9:11300..35500hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3824201
hg1924201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119253
Supporting Variants
SamplesKWS1
Known GenesDDX11L5, FAM138C, WASH1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959689
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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