A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3336



Internal ID15201249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:23823444..23868306hg38UCSC Ensembl
Outerchr20:23804081..23848943hg19UCSC Ensembl
Outerchr20:23752081..23796943hg18UCSC Ensembl
Outerchr20:23752081..23796943hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3844863
hg1944863
hg1844863
hg1744863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5876
SamplesNA19129
Known GenesCST2
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)nsv3336
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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