A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642048



Internal ID7028818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27786844..27800500hg38UCSC Ensembl
Innerchr18:27786870..27800475hg38UCSC Ensembl
Outerchr18:27786819..27800526hg38UCSC Ensembl
chr18:25366808..25380464hg19UCSC Ensembl
Innerchr18:25366834..25380439hg19UCSC Ensembl
Outerchr18:25366783..25380490hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3813657
hg1913657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv609e214
Supporting Variantsessv15827215
SamplesHG01795
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642048
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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