A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979477



Internal ID22754412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59206421..59206421hg38UCSC Ensembl
chr16:59240325..59240325hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979477
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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