A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644945



Internal ID7031696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:314180..315005hg38UCSC Ensembl
Innerchr20:314230..314955hg38UCSC Ensembl
Outerchr20:314130..315055hg38UCSC Ensembl
chr20:294824..295649hg19UCSC Ensembl
Innerchr20:294874..295599hg19UCSC Ensembl
Outerchr20:294774..295699hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16107564, essv16107563
SamplesHG03189, HG03469
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644945
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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