A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645206



Internal ID7031957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10285663..10287551hg38UCSC Ensembl
Innerchr20:10285663..10287551hg38UCSC Ensembl
Outerchr20:10285537..10287669hg38UCSC Ensembl
chr20:10266311..10268199hg19UCSC Ensembl
Innerchr20:10266311..10268199hg19UCSC Ensembl
Outerchr20:10266185..10268317hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg381889
hg191889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16141898
SamplesHG01709
Known GenesSNAP25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645206
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