A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7812



Internal ID15536052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:58668161..58713422hg38UCSC Ensembl
Outerchr3:58653888..58699149hg19UCSC Ensembl
Outerchr3:58628928..58674189hg18UCSC Ensembl
Outerchr3:58628928..58674189hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3845262
hg1945262
hg1845262
hg1745262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3840
Supporting Variants
SamplesNA12156
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)nssv7812
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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