A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119153



Internal ID19258409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:77200..83700hg38UCSC Ensembl
Outerchr8:27200..33700hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg386501
hg196501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981959
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119153
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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