A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1670



Internal ID15198709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:41325144..41809712hg38UCSC Ensembl
Outerchr3:41366635..41851204hg19UCSC Ensembl
Outerchr3:41341639..41826208hg18UCSC Ensembl
Outerchr3:41341639..41826208hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38484569
hg19484570
hg18484570
hg17484570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3779
Supporting Variants
SamplesNA19240
Known GenesULK4
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)nssv1670
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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