A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355



Internal ID15551256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:113697075..113741841hg38UCSC Ensembl
Outerchr8:114709304..114754070hg19UCSC Ensembl
Outerchr8:114778480..114823246hg18UCSC Ensembl
Outerchr8:114778480..114823246hg17UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3844767
hg1944767
hg1844767
hg1744767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8541
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)nsv6355
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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