A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037330



Internal ID21946673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47860038..47860090hg38UCSC Ensembl
chr16:47893949..47894001hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037330
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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