A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261



Internal ID15551153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:74444215..74484663hg38UCSC Ensembl
Outerchr8:75356450..75396898hg19UCSC Ensembl
Outerchr8:75519005..75559453hg18UCSC Ensembl
Outerchr8:75519005..75559453hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3840449
hg1940449
hg1840449
hg1740449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1754, nssv4613
SamplesNA18555, 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)nsv6261
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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