A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962846



Internal ID19206696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:9594690..9596990hg38UCSC Ensembl
Outerchr8:9452200..9454500hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129404
Supporting Variants
SamplesKWS1
Known GenesTNKS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962846
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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