A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10642



Internal ID15542156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:128448696..128460807hg38UCSC Ensembl
Outerchr8:129460942..129473053hg19UCSC Ensembl
Outerchr8:129530124..129542235hg18UCSC Ensembl
Outerchr8:129530124..129542235hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3812112
hg1912112
hg1812112
hg1712112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391
Supporting Variants
SamplesNA18956
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)nssv10642
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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