A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6033



Internal ID15537831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:152110710..152150858hg38UCSC Ensembl
Outerchr5:151490271..151530419hg19UCSC Ensembl
Outerchr5:151470464..151510612hg18UCSC Ensembl
Outerchr5:151470464..151510612hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3840149
hg1940149
hg1840149
hg1740149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5072
Supporting Variants
SamplesNA12156
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)nssv6033
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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