A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667923



Internal ID9587342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10546892..10547113hg38UCSC Ensembl
Outerchr18:10546855..10547163hg38UCSC Ensembl
Innerchr18:10546889..10547110hg19UCSC Ensembl
Outerchr18:10546852..10547160hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5597165, essv6559475
SamplesNA19720, NA18973
Known GenesNAPG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667923
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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