A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625393



Internal ID6665540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12389155..12428448hg38UCSC Ensembl
chr11:12410702..12449995hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3839294
hg1939294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14031927
SamplesHG03709
Known GenesPARVA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625393
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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