A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584984



Internal ID21533528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29059607..29059833hg38UCSC Ensembl
chr16:29070928..29071154hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095299
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584984
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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