A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9412



Internal ID15540363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:114906065..114952700hg38UCSC Ensembl
Outerchr5:114241762..114288397hg19UCSC Ensembl
Outerchr5:114269661..114316296hg18UCSC Ensembl
Outerchr5:114269661..114316296hg17UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3846636
hg1946636
hg1846636
hg1746636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4963
Supporting Variants
SamplesNA18517
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)nssv9412
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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