A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956281



Internal ID22731473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50317415..50320088hg38UCSC Ensembl
chr20:48933952..48936625hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg382674
hg192674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956281
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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