A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639986



Internal ID7026764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13185670..13207607hg38UCSC Ensembl
chr17:13088987..13110924hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3821938
hg1921938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15614703
SamplesNA20760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639986
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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