A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091950



Internal ID21486082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65486095..65486415hg38UCSC Ensembl
chr16:65519998..65520318hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589416
Supporting Variants
SamplesNA12878
Known GenesLINC00922
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091950
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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