A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv879018



Internal ID6286029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:54721518..55022796hg19UCSC Ensembl
Outerchr4:54714753..55030375hg19UCSC Ensembl
Innerchr4:54416275..54717553hg18UCSC Ensembl
Outerchr4:54409510..54725132hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1556253
SamplesMS21868
Known GenesCHIC2, GSX2, RPL21P44
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv879018
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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