A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7663



Internal ID15536201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:21601087..21633543hg38UCSC Ensembl
Outerchr20:21581725..21614181hg19UCSC Ensembl
Outerchr20:21529725..21562181hg18UCSC Ensembl
Outerchr20:21529725..21562181hg17UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3832457
hg1932457
hg1832457
hg1732457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3327
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)nssv7663
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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