A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4953n71



Internal ID6322573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30075052..30150549hg19UCSC Ensembl
chr22:28405052..28480549hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv914963, nsv914964, nsv914966
SamplesMS10311, IS33504, MS18276
Known GenesCABP7, NF2, ZMAT5
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv4953n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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