A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15753510



Internal ID4709094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79908122..79911302hg38UCSC Ensembl
Innerchr17:79908182..79911243hg38UCSC Ensembl
Outerchr17:79908063..79911362hg38UCSC Ensembl
chr17:77881921..77885101hg19UCSC Ensembl
Innerchr17:77881981..77885042hg19UCSC Ensembl
Outerchr17:77881862..77885161hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg383181
hg193181
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641357
Supporting Variants
SamplesHG04227
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15753510
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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