A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002931



Internal ID19190797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:9640330..9643465hg38UCSC Ensembl
Outerchr8:9497840..9500975hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383136
hg193136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151510
Supporting Variants
SamplesKWB1
Known GenesTNKS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002931
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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