A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15900881



Internal ID5902697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61916660..61918424hg38UCSC Ensembl
Innerchr18:61916677..61918408hg38UCSC Ensembl
Outerchr18:61916644..61918441hg38UCSC Ensembl
chr18:59583893..59585657hg19UCSC Ensembl
Innerchr18:59583910..59585641hg19UCSC Ensembl
Outerchr18:59583877..59585674hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg381765
hg191765
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642739
Supporting Variants
SamplesNA19063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15900881
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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