A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589868



Internal ID6977198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14027358..14194080hg38UCSC Ensembl
Innerchr2:14027378..14194061hg38UCSC Ensembl
Outerchr2:14027339..14194100hg38UCSC Ensembl
chr2:14167483..14334204hg19UCSC Ensembl
Innerchr2:14167503..14334185hg19UCSC Ensembl
Outerchr2:14167464..14334224hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38166723
hg19166722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10414261
SamplesHG01357
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589868
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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