A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4438n71



Internal ID6322058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220286142..220505265hg19UCSC Ensembl
chr2:219994386..220213509hg18UCSC 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 Variantsnsv875872, nsv875873
SamplesMS10311, IS35484, MS18276
Known GenesACCN4, CHPF, DES, GMPPA, INHA, MIR3132, OBSL1, SLC4A3, SPEG, STK11IP, TMEM198
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv4438n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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