A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642032



Internal ID7028802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26980559..26983786hg38UCSC Ensembl
Innerchr18:26980567..26983779hg38UCSC Ensembl
Outerchr18:26980552..26983794hg38UCSC Ensembl
chr18:24560523..24563750hg19UCSC Ensembl
Innerchr18:24560531..24563743hg19UCSC Ensembl
Outerchr18:24560516..24563758hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383228
hg193228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15824599
SamplesHG01806
Known GenesCHST9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642032
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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