A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422



Internal ID15551330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:139414720..139459758hg38UCSC Ensembl
Outerchr8:140426963..140472001hg19UCSC Ensembl
Outerchr8:140496145..140541183hg18UCSC Ensembl
Outerchr8:140496145..140541183hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3845039
hg1945039
hg1845039
hg1745039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8566
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)nsv6422
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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