A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963808



Internal ID19220707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:36810878..36810950hg38UCSC Ensembl
Outerchr14:37280083..37280155hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116740
Supporting Variants
SamplesKWS1
Known GenesSLC25A21
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963808
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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