A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435



Internal ID15550244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:109311832..109347924hg38UCSC Ensembl
Outerchr6:109633035..109669127hg19UCSC Ensembl
Outerchr6:109739728..109775820hg18UCSC Ensembl
Outerchr6:109739728..109775820hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3836093
hg1936093
hg1836093
hg1736093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6083
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)nsv5435
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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