A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962072



Internal ID19224650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:16441864..16443652hg38UCSC Ensembl
Outerchr4:16443487..16445275hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg381789
hg191789
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120475
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962072
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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