A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736825



Internal ID20512778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59131753..59132019hg38UCSC Ensembl
chr1:59597425..59597691hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292106
Samples
Known GenesHSD52
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736825
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