A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597129



Internal ID6984443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99052037..99180176hg38UCSC Ensembl
chr3:98770881..98899020hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38128140
hg19128140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11078864, essv11078863, essv11078865
SamplesHG03680, HG03922, HG03882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597129
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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