A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14109700



Internal ID1155660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42423575..42475447hg38UCSC Ensembl
chr11:42445125..42496997hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3851873
hg1951873
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626115
Supporting Variants
SamplesHG01031
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14109700
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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