A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968965



Internal ID18879799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:49783307..49783371hg38UCSC Ensembl
Outerchr14:50250025..50250089hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113648
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968965
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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