A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642198



Internal ID7028968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35294827..35306701hg38UCSC Ensembl
Innerchr18:35294845..35306683hg38UCSC Ensembl
Outerchr18:35294809..35306719hg38UCSC Ensembl
chr18:32874791..32886665hg19UCSC Ensembl
Innerchr18:32874809..32886647hg19UCSC Ensembl
Outerchr18:32874773..32886683hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3811875
hg1911875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842012
SamplesHG02736
Known GenesZNF271
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642198
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