A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7394



Internal ID15536470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:47655526..47700257hg38UCSC Ensembl
Outerchr18:45181897..45226628hg19UCSC Ensembl
Outerchr18:43435895..43480626hg18UCSC Ensembl
Outerchr18:43435895..43480626hg17UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3844732
hg1944732
hg1844732
hg1744732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2286
Supporting Variants
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)nssv7394
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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