A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642285



Internal ID7029055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39745766..39749395hg38UCSC Ensembl
Innerchr18:39745804..39749357hg38UCSC Ensembl
Outerchr18:39745728..39749433hg38UCSC Ensembl
chr18:37325730..37329359hg19UCSC Ensembl
Innerchr18:37325768..37329321hg19UCSC Ensembl
Outerchr18:37325692..37329397hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg383630
hg193630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15846820
SamplesHG03790
Known GenesLINC00669
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642285
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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