A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996977



Internal ID21906320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32668807..32681625hg38UCSC Ensembl
chr4:32670429..32683247hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3812819
hg1912819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547793
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996977
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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