A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976928



Internal ID22751863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24664627..24664627hg38UCSC Ensembl
chr16:24675948..24675948hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388340
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976928
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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