A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966060



Internal ID18882535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:31713730..31714091hg38UCSC Ensembl
Outerchr8:31571246..31571607hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130151
Supporting Variants
SamplesKWS2
Known GenesNRG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966060
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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