A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5915847



Internal ID8893250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35372135..35378135hg38UCSC Ensembl
chr18:32952099..32958099hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660816
Supporting Variants
SamplesHG00330
Known GenesZNF396
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5915847
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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