A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv698e214



Internal ID22756592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57151566..57224682hg38UCSC Ensembl
chr2:57378701..57451817hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3873117
hg1973117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3590914, esv3590911
SamplesHG02450
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv698e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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