A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2333



Internal ID15546896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:62543850..62589422hg38UCSC Ensembl
Outerchr18:60211083..60256655hg19UCSC Ensembl
Outerchr18:58362063..58407635hg18UCSC Ensembl
Outerchr18:58362063..58407635hg17UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3845573
hg1945573
hg1845573
hg1745573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6763
SamplesNA12156
Known GenesZCCHC2
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)nsv2333
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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