A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4660



Internal ID15196520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34200537..34244945hg38UCSC Ensembl
Outerchr20:32788343..32832751hg19UCSC Ensembl
Outerchr20:32252004..32296412hg18UCSC Ensembl
Outerchr20:32252004..32296412hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3844409
hg1944409
hg1844409
hg1744409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3357
Supporting Variants
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)nssv4660
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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