A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3393



Internal ID15201312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:45903113..45913226hg38UCSC Ensembl
Outerchr20:44531752..44541865hg19UCSC Ensembl
Outerchr20:43965159..43975272hg18UCSC Ensembl
Outerchr20:43965159..43975272hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3810114
hg1910114
hg1810114
hg1710114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7685
SamplesNA12156
Known GenesPLTP
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)nsv3393
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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