A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031955



Internal ID21941298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12879566..12883132hg38UCSC Ensembl
chr16:12973423..12976989hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg383567
hg193567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600519
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031955
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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