A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031066



Internal ID21940409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84124854..84124915hg38UCSC Ensembl
chr16:84158459..84158520hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632516
Samples
Known GenesHSDL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031066
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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