A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963682



Internal ID18879483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:13368776..13369053hg38UCSC Ensembl
Outerchr19:13479590..13479867hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111543
Supporting Variants
SamplesKWS2
Known GenesCACNA1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963682
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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