A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8512



Internal ID15535352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:73220525..73265280hg38UCSC Ensembl
Outerchr8:74132760..74177515hg19UCSC Ensembl
Outerchr8:74295314..74340069hg18UCSC Ensembl
Outerchr8:74295314..74340069hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3844756
hg1944756
hg1844756
hg1744756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257
Supporting Variants
SamplesNA12156
Known GenesLOC100130301
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)nssv8512
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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