A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092068



Internal ID21501450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2362366..2362366hg38UCSC Ensembl
chr16:2412367..2412367hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656036
Supporting Variants
SamplesNA19239
Known GenesABCA17P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092068
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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