A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6468352



Internal ID9445756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36399878..36401608hg38UCSC Ensembl
chr18:33979841..33981571hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg381731
hg191731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656572
Supporting Variants
SamplesHG00651
Known GenesFHOD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6468352
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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