A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087837



Internal ID21464807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58741648..58741648hg38UCSC Ensembl
chr16:58775552..58775552hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660119
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087837
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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