A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949219



Internal ID22724670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60536614..60549807hg38UCSC Ensembl
chr20:59111672..59124865hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3813194
hg1913194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949219
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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