A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582



Internal ID15550406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:163969321..163984695hg38UCSC Ensembl
Outerchr6:164390353..164405727hg19UCSC Ensembl
Outerchr6:164310343..164325717hg18UCSC Ensembl
Outerchr6:164360764..164376138hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3815375
hg1915375
hg1815375
hg1715375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8325
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)nsv5582
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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