A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960177



Internal ID19210225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39808782..39823182hg38UCSC Ensembl
Outerchr9:41953800..41968200hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814401
hg1914401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110524
Supporting Variants
SamplesKWS1
Known GenesKGFLP2, MGC21881
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960177
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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