A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8465



Internal ID15535399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:9332290..9377231hg38UCSC Ensembl
Outerchr8:9189800..9234741hg19UCSC Ensembl
Outerchr8:9227210..9272151hg18UCSC Ensembl
Outerchr8:9227210..9272151hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3844942
hg1944942
hg1844942
hg1744942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073
Supporting Variants
SamplesNA12156
Known GenesLOC157273
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)nssv8465
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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