A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641327



Internal ID7028101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78282911..78288396hg38UCSC Ensembl
Innerchr17:78282941..78288367hg38UCSC Ensembl
Outerchr17:78282882..78288426hg38UCSC Ensembl
chr17:76278992..76284477hg19UCSC Ensembl
Innerchr17:76279022..76284448hg19UCSC Ensembl
Outerchr17:76278963..76284507hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg385486
hg195486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15749479
SamplesNA20581
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641327
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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