A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16158080



Internal ID3310866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21828229..21829227hg38UCSC Ensembl
Innerchr20:21828385..21829177hg38UCSC Ensembl
Outerchr20:21828141..21829315hg38UCSC Ensembl
chr20:21808867..21809865hg19UCSC Ensembl
Innerchr20:21809023..21809815hg19UCSC Ensembl
Outerchr20:21808779..21809953hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645497
Supporting Variants
SamplesHG02947
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16158080
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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