A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960084



Internal ID19206871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:158085848..158089848hg38UCSC Ensembl
Outerchr4:159007000..159011000hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg384001
hg194001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110433
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960084
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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