A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736882



Internal ID20512835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57797739..57797791hg38UCSC Ensembl
chr17:55875100..55875152hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736882
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer