A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642343



Internal ID7029113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41893589..41899885hg38UCSC Ensembl
Innerchr18:41893589..41899885hg38UCSC Ensembl
Outerchr18:41893532..41899939hg38UCSC Ensembl
chr18:39473554..39479850hg19UCSC Ensembl
Innerchr18:39473554..39479850hg19UCSC Ensembl
Outerchr18:39473497..39479904hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg386297
hg196297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15855564
SamplesHG02427
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642343
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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