A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038524



Internal ID21947867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62485176..62485421hg38UCSC Ensembl
chr16:62519080..62519325hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038524
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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