A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402216



Internal ID22460086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29967716..30032657hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3864942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402216
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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