A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038745



Internal ID21948088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31016819..31021078hg38UCSC Ensembl
chr16:31028140..31032399hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg384260
hg194260
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038745
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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