A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv360



Internal ID15201539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64864923..64892164hg38UCSC Ensembl
Outerchr11:64632395..64659636hg19UCSC Ensembl
Outerchr11:64388971..64416212hg18UCSC Ensembl
Outerchr11:64388971..64416212hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3827242
hg1927242
hg1827242
hg1727242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8926
SamplesNA12156
Known GenesEHD1, MIR192, MIR194-2
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)nsv360
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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