A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639990



Internal ID7026768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13388273..13402071hg38UCSC Ensembl
chr17:13291590..13305388hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3813799
hg1913799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15614708
SamplesNA19681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639990
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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