A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600020



Internal ID21548658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19494994..19495312hg38UCSC Ensembl
chr16:19506316..19506634hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093807
SamplesHG00731
Known GenesTMC5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600020
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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