A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263035



Internal ID20472253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225970268..225970425hg38UCSC Ensembl
chr1:226157968..226158125hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738873
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263035
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