A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643149



Internal ID7029918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75742142..75767774hg38UCSC Ensembl
Innerchr18:75742142..75767774hg38UCSC Ensembl
Outerchr18:75741642..75768274hg38UCSC Ensembl
chr18:73454097..73479729hg19UCSC Ensembl
Innerchr18:73454097..73479729hg19UCSC Ensembl
Outerchr18:73453597..73480229hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3825633
hg1925633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv640e214
Supporting Variantsessv15935907, essv15935909, essv15935908
SamplesNA06984, HG03061, HG03703
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643149
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer