A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16221010



Internal ID1924018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62429953..62456719hg38UCSC Ensembl
chr20:61005009..61031775hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3826767
hg1926767
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3646291
Supporting Variants
SamplesHG01798
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16221010
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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