A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595927



Internal ID6983245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39532822..39559492hg38UCSC Ensembl
chr3:39574313..39600983hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3826671
hg1926671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10987753, essv10987754, essv10987755
SamplesHG02923, HG03198, HG03265
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595927
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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