A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591437



Internal ID6978765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80938578..80966132hg38UCSC Ensembl
chr2:81165702..81193256hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3827555
hg1927555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10559528
SamplesHG02837
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591437
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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