A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023606



Internal ID21932949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28088983..28089154hg38UCSC Ensembl
chr16:28100304..28100475hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023606
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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