A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5886



Internal ID15543499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:55821527..55866110hg38UCSC Ensembl
Outerchr20:54396583..54441166hg19UCSC Ensembl
Outerchr20:53829990..53874573hg18UCSC Ensembl
Outerchr20:53829990..53874573hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3844584
hg1944584
hg1844584
hg1744584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3420
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)nssv5886
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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