A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625306



Internal ID6665454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7871961..7946682hg38UCSC Ensembl
chr11:7893508..7968229hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3874722
hg1974722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14017996, essv14017997, essv14017995
SamplesHG01853, NA19445, NA19454
Known GenesLOC283299, OR10A3, OR10A6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625306
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer