A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642797



Internal ID7029566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:64359425..64421380hg38UCSC Ensembl
Innerchr18:64359466..64421339hg38UCSC Ensembl
Outerchr18:64359384..64421421hg38UCSC Ensembl
chr18:62026660..62088615hg19UCSC Ensembl
Innerchr18:62026701..62088574hg19UCSC Ensembl
Outerchr18:62026619..62088656hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3861956
hg1961956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15906905
SamplesHG03603
Known GenesLOC284294
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642797
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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