A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625083



Internal ID6665235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:851409..1030159hg38UCSC Ensembl
chr11:851409..1030159hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38178751
hg19178751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv175e214
Supporting Variantsessv13992145
SamplesHG03830
Known GenesAP2A2, CHID1, MUC6, TSPAN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625083
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