A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642829



Internal ID7029598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65460753..65511881hg38UCSC Ensembl
Innerchr18:65461253..65511381hg38UCSC Ensembl
Outerchr18:65459753..65512881hg38UCSC Ensembl
chr18:63127989..63179117hg19UCSC Ensembl
Innerchr18:63128489..63178617hg19UCSC Ensembl
Outerchr18:63126989..63180117hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3851129
hg1951129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv624e214
Supporting Variantsessv15909555, essv15909556
SamplesNA20812, NA19722
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642829
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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