A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8522



Internal ID15535342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:87908507..87953144hg38UCSC Ensembl
Outerchr8:88920735..88965372hg19UCSC Ensembl
Outerchr8:88989851..89034488hg18UCSC Ensembl
Outerchr8:88989851..89034488hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3844638
hg1944638
hg1844638
hg1744638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6292
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)nssv8522
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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