A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405232



Internal ID22463102
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 StatusS
Merged Variantsnsv5956281
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405232
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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