A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671542



Internal ID9590961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22619192..22888319hg38UCSC Ensembl
Outerchr18:22619158..22888354hg38UCSC Ensembl
Innerchr18:20199155..20468282hg19UCSC Ensembl
Outerchr18:20199121..20468317hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38269197
hg19269197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv585e199
Supporting Variantsessv5595204
SamplesNA19713
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671542
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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