A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969531



Internal ID22744466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41629256..41629256hg38UCSC Ensembl
chr20:40257895..40257895hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969531
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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