A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596462



Internal ID6983777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67529615..67591822hg38UCSC Ensembl
chr3:67580039..67642246hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3862208
hg1962208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11031092
SamplesHG02464
Known GenesSUCLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596462
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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