A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993684



Internal ID19227907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:101463933..101464023hg38UCSC Ensembl
Outerchr14:101930270..101930360hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142177
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993684
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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