A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069



Internal ID15545632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:62731774..63069926hg38UCSC Ensembl
Outerchr13:63305907..63644059hg19UCSC Ensembl
Outerchr13:62203908..62542060hg18UCSC Ensembl
Outerchr13:62203908..62542060hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38338153
hg19338153
hg18338153
hg17338153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9995, nssv9135
SamplesNA12156, NA18956
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)nsv1069
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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