A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4951n71



Internal ID6322571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29696438..29714069hg19UCSC Ensembl
chr22:28026438..28044069hg18UCSC 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 Variantsnsv914960, nsv914959
SamplesSP54956, SP54043, SP54988
Known GenesEWSR1, GAS2L1, RASL10A
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv4951n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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