A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982283



Internal ID18873031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:98426572..98427472hg38UCSC Ensembl
Outerchr8:99438800..99439700hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145198
Supporting Variants
SamplesKWS1
Known GenesKCNS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982283
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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