A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032847



Internal ID21942190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51228834..51228902hg38UCSC Ensembl
chr16:51262745..51262813hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032847
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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