A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5971324



Internal ID9064064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9284981..9286148hg38UCSC Ensembl
chr18:9284979..9286146hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381168
hg191168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657711
Supporting Variants
SamplesHG00731
Known GenesANKRD12
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5971324
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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