A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081758



Internal ID21452194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57423535..57423535hg38UCSC Ensembl
chr16:57457447..57457447hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646147
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081758
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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