A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502



Internal ID15551418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:22487567..22518349hg38UCSC Ensembl
Outerchr9:22487566..22518348hg19UCSC Ensembl
Outerchr9:22477566..22508348hg18UCSC Ensembl
Outerchr9:22477566..22508348hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3830783
hg1930783
hg1830783
hg1730783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707, nssv6266
SamplesNA12156, NA12878
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)nsv6502
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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