A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv911782



Internal ID6273709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42500373..42887492hg19UCSC Ensembl
Outerchr19:42489516..42931004hg19UCSC Ensembl
Innerchr19:47192213..47579332hg18UCSC Ensembl
Outerchr19:47181356..47622844hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1586081
SamplesIS37646
Known GenesATP1A3, CIC, CNFN, DEDD2, ERF, GRIK5, GSK3A, LIPE, LOC100505622, MEGF8, MIR4323, PAFAH1B3, POU2F2, PRR19, TMEM145, ZNF526, ZNF574
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv911782
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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