A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6256



Internal ID15537607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:134064608..134077910hg38UCSC Ensembl
Outerchr8:135076851..135090153hg19UCSC Ensembl
Outerchr8:135146033..135159335hg18UCSC Ensembl
Outerchr8:135146033..135159335hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3813303
hg1913303
hg1813303
hg1713303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407
Supporting Variants
SamplesNA12156
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)nssv6256
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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