A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526259



Internal ID20899620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34877493..34880382hg38UCSC Ensembl
chr20:33465296..33468185hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382890
hg192890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067971
Samples
Known GenesACSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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