A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642751



Internal ID7029520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62665974..62687029hg38UCSC Ensembl
Innerchr18:62666474..62686529hg38UCSC Ensembl
Outerchr18:62664974..62688029hg38UCSC Ensembl
chr18:60333207..60354262hg19UCSC Ensembl
Innerchr18:60333707..60353762hg19UCSC Ensembl
Outerchr18:60332207..60355262hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3821056
hg1921056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15903260
SamplesHG02613
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642751
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer