A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5972



Internal ID15543395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:68582185..68600578hg38UCSC Ensembl
Outerchr3:68631336..68649729hg19UCSC Ensembl
Outerchr3:68714026..68732419hg18UCSC Ensembl
Outerchr3:68714026..68732419hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3818394
hg1918394
hg1818394
hg1718394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3862
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)nssv5972
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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