A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565



Internal ID15550387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1966686..1995138hg38UCSC Ensembl
Outerchr10:2008880..2037332hg19UCSC Ensembl
Outerchr10:1998880..2027332hg18UCSC Ensembl
Outerchr10:1998880..2027332hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3811038
hg1911038
hg1811038
hg1711038
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10625
SamplesNA18956
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)nsv5565
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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