A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625358



Internal ID6665505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10435119..10512909hg38UCSC Ensembl
chr11:10456666..10534456hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3877791
hg1977791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14028067
SamplesHG03875
Known GenesAMPD3, MIR4485, MTRNR2L8, RNF141
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625358
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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