A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2366



Internal ID15546929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:77800629..77829540hg38UCSC Ensembl
Outerchr18:75512585..75541496hg19UCSC Ensembl
Outerchr18:73641573..73670484hg18UCSC Ensembl
Outerchr18:73641573..73670484hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3828912
hg1928912
hg1828912
hg1728912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7418
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)nsv2366
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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