A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8497



Internal ID15535367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:56782343..56827634hg38UCSC Ensembl
Outerchr8:57694902..57740193hg19UCSC Ensembl
Outerchr8:57857456..57902747hg18UCSC Ensembl
Outerchr8:57857456..57902747hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3845292
hg1945292
hg1845292
hg1745292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6204
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)nssv8497
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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