A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642702



Internal ID7029471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60471756..60494972hg38UCSC Ensembl
Innerchr18:60472256..60494472hg38UCSC Ensembl
Outerchr18:60470756..60495972hg38UCSC Ensembl
chr18:58138989..58162205hg19UCSC Ensembl
Innerchr18:58139489..58161705hg19UCSC Ensembl
Outerchr18:58137989..58163205hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3823217
hg1923217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15898295
SamplesHG02586
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642702
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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