A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641178



Internal ID7027952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71736827..71745933hg38UCSC Ensembl
Innerchr17:71736844..71745917hg38UCSC Ensembl
Outerchr17:71736811..71745950hg38UCSC Ensembl
chr17:69732968..69742074hg19UCSC Ensembl
Innerchr17:69732985..69742058hg19UCSC Ensembl
Outerchr17:69732952..69742091hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg389107
hg199107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15734792
SamplesHG01865
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641178
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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