A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023890



Internal ID21933233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30679456..30679760hg38UCSC Ensembl
chr16:30690777..30691081hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023890
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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