A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16179974



Internal ID981499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37263192..37265861hg38UCSC Ensembl
Innerchr20:37263197..37265857hg38UCSC Ensembl
Outerchr20:37263188..37265866hg38UCSC Ensembl
chr20:35891595..35894264hg19UCSC Ensembl
Innerchr20:35891600..35894260hg19UCSC Ensembl
Outerchr20:35891591..35894269hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg382670
hg192670
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645755
Supporting Variants
SamplesHG00610
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16179974
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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