A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2331



Internal ID15194125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34227211..34236042hg38UCSC Ensembl
Outerchr20:32815017..32823848hg19UCSC Ensembl
Outerchr20:32278678..32287509hg18UCSC Ensembl
Outerchr20:32278678..32287509hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg388832
hg198832
hg188832
hg178832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3357
Supporting Variants
SamplesNA18555
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)nssv2331
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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