A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031906



Internal ID21941249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4078779..4087306hg38UCSC Ensembl
chr16:4128780..4137307hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388528
hg198528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616100
Samples
Known GenesADCY9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031906
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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