A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662069



Internal ID21610374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54338503..54338503hg38UCSC Ensembl
chr16:54372415..54372415hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098597
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662069
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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