A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6161



Internal ID15551043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:37905168..37931720hg38UCSC Ensembl
Outerchr8:37762686..37789238hg19UCSC Ensembl
Outerchr8:37881844..37908396hg18UCSC Ensembl
Outerchr8:37881844..37908396hg17UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3812730
hg1912730
hg1812730
hg1712730
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5079
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)nsv6161
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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