A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595939



Internal ID6983257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39872952..39884999hg38UCSC Ensembl
chr3:39914443..39926490hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3812048
hg1912048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10987893, essv10987889, essv10987892, essv10987887, essv10987894, essv10987890, essv10987891, essv10987888
SamplesHG04158, NA20805, HG03976, HG04182, HG03928, HG04155, HG04063, HG04134
Known GenesMYRIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595939
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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