A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515



Internal ID15549930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:119487546..119532157hg38UCSC Ensembl
Outerchr11:119358258..119402867hg19UCSC Ensembl
Outerchr11:118863468..118908077hg18UCSC Ensembl
Outerchr11:118863468..118908077hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3844612
hg1944610
hg1844610
hg1744610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4627
SamplesNA19129
Known GenesUSP2-AS1
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)nsv515
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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