A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv911282



Internal ID6273209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18638405..18915988hg19UCSC Ensembl
Outerchr19:18624964..18928480hg19UCSC Ensembl
Innerchr19:18499405..18776988hg18UCSC Ensembl
Outerchr19:18485964..18789480hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1532530
SamplesMS10769
Known GenesC19orf50, C19orf60, COMP, CRLF1, CRTC1, ELL, FKBP8, KLHL26, TMEM59L, UBA52
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv911282
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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