A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15906737



Internal ID4065604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63810723..63845113hg38UCSC Ensembl
Innerchr18:63810759..63845078hg38UCSC Ensembl
Outerchr18:63810688..63845149hg38UCSC Ensembl
chr18:61477957..61512347hg19UCSC Ensembl
Innerchr18:61477993..61512312hg19UCSC Ensembl
Outerchr18:61477922..61512383hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3834391
hg1934391
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642782
Supporting Variants
SamplesHG03702
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15906737
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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