A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11062



Internal ID15539646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:68684720..68719913hg38UCSC Ensembl
Outerchr3:68733871..68769064hg19UCSC Ensembl
Outerchr3:68816561..68851754hg18UCSC Ensembl
Outerchr3:68816561..68851754hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3835194
hg1935194
hg1835194
hg1735194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3863
Supporting Variants
SamplesNA15510
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)nssv11062
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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