A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961865



Internal ID19223353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:101463969..101464061hg38UCSC Ensembl
Outerchr14:101930306..101930398hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120303
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961865
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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