A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641657



Internal ID6681742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5636804..5643584hg38UCSC Ensembl
Innerchr18:5636804..5643584hg38UCSC Ensembl
Outerchr18:5636608..5643791hg38UCSC Ensembl
chr18:5636803..5643583hg19UCSC Ensembl
Innerchr18:5636803..5643583hg19UCSC Ensembl
Outerchr18:5636607..5643790hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386781
hg196781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15792842
SamplesHG02382
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641657
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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