A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15728029



Internal ID3758562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67819504..67821118hg38UCSC Ensembl
Innerchr17:67819524..67821099hg38UCSC Ensembl
Outerchr17:67819485..67821138hg38UCSC Ensembl
chr17:65815620..65817234hg19UCSC Ensembl
Innerchr17:65815640..65817215hg19UCSC Ensembl
Outerchr17:65815601..65817254hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381615
hg191615
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641101
Supporting Variants
SamplesHG03388
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15728029
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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