A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625299



Internal ID6665447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7691697..7778807hg38UCSC Ensembl
chr11:7712928..7800354hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3887111
hg1987427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv184e214
Supporting Variantsessv14015579, essv14015578
SamplesHG01853, HG01435
Known GenesOVCH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625299
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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