A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139



Internal ID15204332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:30146815..30192125hg38UCSC Ensembl
Outerchr8:30004331..30049641hg19UCSC Ensembl
Outerchr8:30123873..30169183hg18UCSC Ensembl
Outerchr8:30123873..30169183hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3845311
hg1945311
hg1845311
hg1745311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8478
SamplesNA12156
Known GenesDCTN6, MIR548O2
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)nsv6139
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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