A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11070



Internal ID15539638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:162791159..162914903hg38UCSC Ensembl
Outerchr3:162508947..162632691hg19UCSC Ensembl
Outerchr3:163991641..164115385hg18UCSC Ensembl
Outerchr3:163991649..164115393hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38123745
hg19123745
hg18123745
hg17123745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4093
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)nssv11070
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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