A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597516



Internal ID6984657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:117301886..117439117hg38UCSC Ensembl
chr3:117020733..117157964hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38137232
hg19137232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11112588
SamplesNA21097
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597516
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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