A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950129



Internal ID22725551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32854686..32854742hg38UCSC Ensembl
chr20:31442492..31442548hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950129
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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