A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4417n71



Internal ID6322037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208969865..208994045hg19UCSC Ensembl
chr2:208678110..208702290hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv875745, nsv875746
SamplesIS33797, SP54988, IS39233
Known GenesCRYGC, CRYGD, LOC100507443
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv4417n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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