A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8235



Internal ID15188943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:36831553..36858434hg38UCSC Ensembl
Outerchr6:36799329..36826210hg19UCSC Ensembl
Outerchr6:36907307..36934188hg18UCSC Ensembl
Outerchr6:36907307..36934188hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3826882
hg1926882
hg1826882
hg1726882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5262
Supporting Variants
SamplesNA12156
Known GenesCPNE5, PPIL1
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)nssv8235
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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