A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085734



Internal ID21458032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64838754..64838861hg38UCSC Ensembl
chr16:64872657..64872764hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591622
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085734
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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