A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426



Internal ID15550234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:105649392..105694571hg38UCSC Ensembl
Outerchr6:106097267..106142446hg19UCSC Ensembl
Outerchr6:106203960..106249139hg18UCSC Ensembl
Outerchr6:106203960..106249139hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3845180
hg1945180
hg1845180
hg1745180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8281
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)nsv5426
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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