A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547304



Internal ID20920506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56058301..56062500hg38UCSC Ensembl
chr20:54633357..54637556hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070390
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547304
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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