A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540572



Internal ID20913861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63841701..63850400hg38UCSC Ensembl
chr20:62473054..62481753hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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