A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082964



Internal ID21506326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11198165..11198165hg38UCSC Ensembl
chr16:11292022..11292022hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657388
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082964
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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