A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038855



Internal ID21948198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:276968..277140hg38UCSC Ensembl
chr16:326968..327140hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038855
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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