A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597528



Internal ID6984669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:117909326..117933515hg38UCSC Ensembl
chr3:117628173..117652362hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3824190
hg1924190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11113048
SamplesNA21097
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597528
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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