A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973347



Internal ID22748282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24778412..24778412hg38UCSC Ensembl
chr20:24759048..24759048hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973347
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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