A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979975



Internal ID19230794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:165509020..165509089hg38UCSC Ensembl
Outerchr4:166430172..166430241hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117402
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979975
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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