A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874936



Internal ID22649890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54665232..54667814hg38UCSC Ensembl
chr16:54699144..54701726hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg382583
hg192583
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471599
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874936
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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