A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034785



Internal ID21944128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57420598..57421281hg38UCSC Ensembl
chr16:57454510..57455193hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622809
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034785
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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