A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4870



Internal ID15543008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:152073599..152085373hg38UCSC Ensembl
Outerchr5:151453160..151464934hg19UCSC Ensembl
Outerchr5:151433353..151445127hg18UCSC Ensembl
Outerchr5:151433353..151445127hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3811775
hg1911775
hg1811775
hg1711775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5071
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)nssv4870
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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