A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6364989



Internal ID9809072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:38997702..39007008hg38UCSC Ensembl
Outerchr18:38997331..39007378hg38UCSC Ensembl
Innerchr18:36577666..36586972hg19UCSC Ensembl
Outerchr18:36577295..36587342hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3810048
hg1910048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672566
Supporting Variants
SamplesNA19914
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6364989
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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