A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961317



Internal ID22736276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56188986..56189162hg38UCSC Ensembl
chr20:54764042..54764218hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961317
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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