A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972325



Internal ID22747260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66126382..66126382hg38UCSC Ensembl
chr16:66160285..66160285hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383200
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972325
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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