A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6155



Internal ID15551036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:36550128..36595223hg38UCSC Ensembl
Outerchr8:36407646..36452741hg19UCSC Ensembl
Outerchr8:36526804..36571899hg18UCSC Ensembl
Outerchr8:36526804..36571899hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3845096
hg1945096
hg1845096
hg1745096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5077
SamplesNA19129
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)nsv6155
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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