A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6168878



Internal ID9802256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:38997528..39005169hg38UCSC Ensembl
Outerchr18:38997491..39005219hg38UCSC Ensembl
Innerchr18:36577492..36585133hg19UCSC Ensembl
Outerchr18:36577455..36585183hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg387729
hg197729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670467
Supporting Variants
SamplesNA19900
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6168878
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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