A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv914604



Internal ID6276531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24220358..24242973hg19UCSC Ensembl
Outerchr22:24212826..24248761hg19UCSC Ensembl
Innerchr22:22550358..22572973hg18UCSC Ensembl
Outerchr22:22542826..22578761hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1592507
SamplesIS39233
Known GenesLOC284889, MIF, SLC2A11
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv914604
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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