A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641229



Internal ID7028003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73831672..73995581hg38UCSC Ensembl
chr17:71827811..71991720hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38163910
hg19163910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15737302, essv15737303
SamplesNA12348, NA06989
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641229
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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