A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641111



Internal ID7027885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68336878..68365487hg38UCSC Ensembl
chr17:66333019..66361628hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3828610
hg1928610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15730494
SamplesHG02283
Known GenesARSG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641111
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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