A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959496



Internal ID19208503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:18223623..18284323hg38UCSC Ensembl
Outerchr14:19000100..19060800hg19UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg3860701
hg1960701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110227
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959496
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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