A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027357



Internal ID21936700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11354045..11354212hg38UCSC Ensembl
chr16:11447902..11448069hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027357
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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