A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642204



Internal ID7028974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35578285..35579469hg38UCSC Ensembl
Innerchr18:35578296..35579458hg38UCSC Ensembl
Outerchr18:35578274..35579480hg38UCSC Ensembl
chr18:33158249..33159433hg19UCSC Ensembl
Innerchr18:33158260..33159422hg19UCSC Ensembl
Outerchr18:33158238..33159444hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842025, essv15842026, essv15842024
SamplesHG00766, HG02371, HG02406
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642204
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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