A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976833



Internal ID19226274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:24412998..24448898hg38UCSC Ensembl
Outerchr19:24595800..24631700hg19UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg3835901
hg1935901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124780
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976833
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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