A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4651



Internal ID15543253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:65764252..65796508hg38UCSC Ensembl
Outerchr2:65991386..66023642hg19UCSC Ensembl
Outerchr2:65844890..65877146hg18UCSC Ensembl
Outerchr2:65903037..65935293hg17UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3832257
hg1932257
hg1832257
hg1732257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2759
Supporting Variants
SamplesNA19129
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)nssv4651
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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