A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4963



Internal ID15549725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:114898734..114952700hg38UCSC Ensembl
Outerchr5:114234431..114288397hg19UCSC Ensembl
Outerchr5:114262330..114316296hg18UCSC Ensembl
Outerchr5:114262330..114316296hg17UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3853967
hg1953967
hg1853967
hg1753967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9412, nssv488, nssv4856
SamplesNA18517, NA19240, NA19129
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)nsv4963
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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