A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6201897



Internal ID9185364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:28693302..28698308hg38UCSC Ensembl
Outerchr18:28692781..28698728hg38UCSC Ensembl
Innerchr18:26273266..26278272hg19UCSC Ensembl
Outerchr18:26272745..26278692hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg385948
hg195948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675548
Supporting Variants
SamplesHG01455
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6201897
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