A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740900



Internal ID20516877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31174103..31175240hg38UCSC Ensembl
chr16:31185424..31186561hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381138
hg191138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740900
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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