A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968759



Internal ID22743694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56691673..56691673hg38UCSC Ensembl
chr20:55266729..55266729hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968759
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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