A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7649



Internal ID15536215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:6861085..6889822hg38UCSC Ensembl
Outerchr20:6841732..6870469hg19UCSC Ensembl
Outerchr20:6789732..6818469hg18UCSC Ensembl
Outerchr20:6789732..6818469hg17UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3828738
hg1928738
hg1828738
hg1728738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3275
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)nssv7649
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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