A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028968



Internal ID21938311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64093269..64144351hg38UCSC Ensembl
chr16:64127173..64178255hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3851083
hg1951083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028968
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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