A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527732



Internal ID20901093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22771719..22779509hg38UCSC Ensembl
chr20:22752357..22760147hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg387791
hg197791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527732
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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