A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130156



Internal ID19278055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:58165877..58166230hg38UCSC Ensembl
Outerchr8:59078436..59078789hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3831n106
Supporting Variantsnssv3966065
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130156
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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