A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10434760



Internal ID436576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26587421..26598916hg38UCSC Ensembl
chr2:26810289..26821784hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3811496
hg1911496
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3590124
Supporting Variants
SamplesHG03775
Known GenesCIB4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10434760
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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