A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961862



Internal ID19218441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:92725684..92725754hg38UCSC Ensembl
Outerchr14:93192029..93192099hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120300
Supporting Variants
SamplesKWS1
Known GenesLGMN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961862
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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