A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5951



Internal ID15543420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:22501239..22545934hg38UCSC Ensembl
Outerchr3:22542730..22587425hg19UCSC Ensembl
Outerchr3:22517734..22562429hg18UCSC Ensembl
Outerchr3:22517734..22562429hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3844696
hg1944696
hg1844696
hg1744696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3730
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)nssv5951
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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