A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625094



Internal ID6665246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1002638..1016158hg38UCSC Ensembl
chr11:1002638..1016158hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3813521
hg1913521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13992183, essv13992182, essv13992181
SamplesHG00626, HG00596, NA12272
Known GenesAP2A2, MUC6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625094
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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