A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997557



Internal ID21906900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51834045..51834106hg38UCSC Ensembl
chr4:52700211..52700272hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997557
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