A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395920



Internal ID22453790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62574396..62575646hg38UCSC Ensembl
chr20:61171603..61172853hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381251
hg191251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395920
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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