A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6400819



Internal ID9883951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74209577..74216225hg38UCSC Ensembl
Outerchr18:74209540..74216275hg38UCSC Ensembl
Innerchr18:71876812..71883460hg19UCSC Ensembl
Outerchr18:71876775..71883510hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg386736
hg196736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667741
Supporting Variants
SamplesNA20759
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6400819
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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