A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4437n71



Internal ID6322057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220286142..220389355hg19UCSC Ensembl
chr2:219994386..220097599hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv875871, nsv875874
SamplesIS33504, MS10769
Known GenesACCN4, DES, GMPPA, SPEG
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv4437n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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