A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10415050



Internal ID416866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14769076..14783048hg38UCSC Ensembl
chr2:14909200..14923172hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3813973
hg1913973
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3589899
Supporting Variants
SamplesHG00375
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10415050
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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