A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524111



Internal ID20897472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:886454..953648hg38UCSC Ensembl
chr20:867097..934291hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3867195
hg1967195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070806
Samples
Known GenesANGPT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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