A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595220



Internal ID6982538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8611079..8688004hg38UCSC Ensembl
chr3:8652765..8729690hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3876926
hg1976926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10917250, essv10917251, essv10917249
SamplesHG01277, HG01149, NA19213
Known GenesSSUH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595220
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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