A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6208



Internal ID15551094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:57432652..57477329hg38UCSC Ensembl
Outerchr8:58345211..58389888hg19UCSC Ensembl
Outerchr8:58507765..58552442hg18UCSC Ensembl
Outerchr8:58507765..58552442hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3844678
hg1944678
hg1844678
hg1744678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5095, nssv8499, nssv9916
SamplesNA18507, NA12156, NA19129
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)nsv6208
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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