A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8369



Internal ID15535495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:46440341..46485511hg38UCSC Ensembl
Outerchr7:46479939..46525109hg19UCSC Ensembl
Outerchr7:46446464..46491634hg18UCSC Ensembl
Outerchr7:46253179..46298349hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3845171
hg1945171
hg1845171
hg1745171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5726
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)nssv8369
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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