A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv586e214



Internal ID22756480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72302777..72303867hg38UCSC Ensembl
chr17:70298918..70300008hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3641193, esv3641192
SamplesNA20869, NA19214
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv586e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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