A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399



Internal ID15551304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:131109890..131155261hg38UCSC Ensembl
Outerchr8:132122137..132167508hg19UCSC Ensembl
Outerchr8:132191319..132236690hg18UCSC Ensembl
Outerchr8:132191319..132236690hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3845372
hg1945372
hg1845372
hg1745372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6255
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)nsv6399
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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