A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625148



Internal ID6665299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3609614..3680474hg38UCSC Ensembl
chr11:3630844..3701704hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3870861
hg1970861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13996709
SamplesNA20509
Known GenesART1, ART5, CHRNA10, NUP98, TRPC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625148
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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