A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028932



Internal ID21938275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57418407..57420488hg38UCSC Ensembl
chr16:57452319..57454400hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382082
hg192082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028932
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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