A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977401



Internal ID22752336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69713893..69713893hg38UCSC Ensembl
chr16:69747796..69747796hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381952
Samples
Known GenesNQO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977401
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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