A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963894



Internal ID18865892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:17315088..17315148hg38UCSC Ensembl
Outerchr19:17425897..17425957hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129618
Supporting Variants
SamplesKWS1
Known GenesDDA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963894
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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