A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16182092



Internal ID6326254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39041198..39066499hg38UCSC Ensembl
chr20:37669841..37695142hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3825302
hg1925302
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645800
Supporting Variants
SamplesNA19921
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16182092
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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