A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972327



Internal ID22747262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43274240..43274240hg38UCSC Ensembl
chr20:41902880..41902880hg19UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972327
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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