A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2641



Internal ID15200518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:24081872..24103374hg38UCSC Ensembl
Outerchr2:24304742..24326244hg19UCSC Ensembl
Outerchr2:24158246..24179748hg18UCSC Ensembl
Outerchr2:24216393..24237895hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3821503
hg1921503
hg1821503
hg1721503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7472
SamplesNA12156
Known GenesTP53I3
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)nsv2641
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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