A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16121917



Internal ID2953458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3410366..3420772hg38UCSC Ensembl
Innerchr20:3410366..3420772hg38UCSC Ensembl
Outerchr20:3409866..3421272hg38UCSC Ensembl
chr20:3391013..3401419hg19UCSC Ensembl
Innerchr20:3391013..3401419hg19UCSC Ensembl
Outerchr20:3390513..3401919hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3810407
hg1910407
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645040
Supporting Variants
SamplesHG02610
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16121917
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