A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4527



Internal ID15539254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:32928796..32950712hg38UCSC Ensembl
Outerchr20:31516602..31538518hg19UCSC Ensembl
Outerchr20:30980263..31002179hg18UCSC Ensembl
Outerchr20:30980263..31002179hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3821917
hg1921917
hg1821917
hg1721917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3350
Supporting Variants
SamplesNA12878
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)nssv4527
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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