A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10453



Internal ID15542345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:58016905..58056919hg38UCSC Ensembl
Outerchr5:57312732..57352746hg19UCSC Ensembl
Outerchr5:57348489..57388503hg18UCSC Ensembl
Outerchr5:57348489..57388503hg17UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3840015
hg1940015
hg1840015
hg1740015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4840
Supporting Variants
SamplesNA18956
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)nssv10453
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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