A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959933



Internal ID19210116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:36629319..36629382hg38UCSC Ensembl
Outerchr20:35257722..35257785hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119489
Supporting Variants
SamplesKWS1
Known GenesSLA2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959933
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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