A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961941



Internal ID22736880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47804993..47806305hg38UCSC Ensembl
chr20:46433737..46435049hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961941
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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