A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9462



Internal ID15540413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:64330012..64360679hg38UCSC Ensembl
Outerchr8:65242569..65273236hg19UCSC Ensembl
Outerchr8:65405123..65435790hg18UCSC Ensembl
Outerchr8:65405123..65435790hg17UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3830668
hg1930668
hg1830668
hg1730668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6230
Supporting Variants
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)nssv9462
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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