A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268938



Internal ID20478156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51590321..51590558hg38UCSC Ensembl
chr1:52055993..52056230hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731049
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268938
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