A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977861



Internal ID19246400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:41186371..41204971hg38UCSC Ensembl
Outerchr9:69259600..69278200hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3818601
hg1918601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125055
Supporting Variants
SamplesKWS2
Known GenesCBWD5, CBWD6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977861
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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