A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592734



Internal ID21541318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48966776..48966859hg38UCSC Ensembl
chr16:49000687..49000770hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097219
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592734
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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