A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6160



Internal ID15551042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:37507258..37541764hg38UCSC Ensembl
Outerchr8:37364776..37399282hg19UCSC Ensembl
Outerchr8:37483934..37518440hg18UCSC Ensembl
Outerchr8:37483934..37518440hg17UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3834507
hg1934507
hg1834507
hg1734507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5078
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)nsv6160
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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