A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641034



Internal ID7027808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64942448..64947826hg38UCSC Ensembl
Innerchr17:64942448..64947826hg38UCSC Ensembl
Outerchr17:64942355..64947900hg38UCSC Ensembl
chr17:62938566..62943944hg19UCSC Ensembl
Innerchr17:62938566..62943944hg19UCSC Ensembl
Outerchr17:62938473..62944018hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg385379
hg195379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15724786
SamplesNA20808
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641034
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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