A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962313



Internal ID19213295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:32198611..32200027hg38UCSC Ensembl
Outerchr14:32667817..32669233hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381417
hg191417
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111099
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962313
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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