A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640756



Internal ID7027530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50903053..50923436hg38UCSC Ensembl
chr17:48980414..49000797hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3820384
hg1920384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15695221, essv15695222
SamplesNA19189, HG02274
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640756
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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