A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528902



Internal ID20902263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2673901..2676000hg38UCSC Ensembl
chr20:2654547..2656646hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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