A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642774



Internal ID7029543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63629999..63636362hg38UCSC Ensembl
Innerchr18:63629999..63636362hg38UCSC Ensembl
Outerchr18:63629801..63636556hg38UCSC Ensembl
chr18:61297233..61303596hg19UCSC Ensembl
Innerchr18:61297233..61303596hg19UCSC Ensembl
Outerchr18:61297035..61303790hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg386364
hg196364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15906712
SamplesHG00634
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642774
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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