A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589888



Internal ID6977218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14479413..14508152hg38UCSC Ensembl
chr2:14619537..14648276hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3828740
hg1928740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10414791
SamplesHG03907
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589888
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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