A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068



Internal ID15545631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:61489045..61534271hg38UCSC Ensembl
Outerchr13:62063178..62108404hg19UCSC Ensembl
Outerchr13:60961179..61006405hg18UCSC Ensembl
Outerchr13:60961179..61006405hg17UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3845227
hg1945227
hg1845227
hg1745227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9133
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)nsv1068
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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