A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351



Internal ID15551252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:112055127..112089703hg38UCSC Ensembl
Outerchr8:113067356..113101932hg19UCSC Ensembl
Outerchr8:113136532..113171108hg18UCSC Ensembl
Outerchr8:113136532..113171108hg17UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3834577
hg1934577
hg1834577
hg1734577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9468
SamplesNA18517
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv6351
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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