A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589856



Internal ID6977186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13711038..13823141hg38UCSC Ensembl
chr2:13851163..13963266hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38112104
hg19112104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10412901
SamplesHG03520
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589856
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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