A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6675n54



Internal ID22774570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5705411..5710632hg38UCSC Ensembl
chr2:5845543..5850764hg19UCSC Ensembl
chr2:5762994..5768215hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg385222
hg195222
hg185222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580883, nsv580872
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6675n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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