A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956796



Internal ID18876491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:31713740..31714076hg38UCSC Ensembl
Outerchr8:31571256..31571592hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117139
Supporting Variants
SamplesKWS1
Known GenesNRG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956796
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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