A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610613



Internal ID21802660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54201879..54203004hg38UCSC Ensembl
chr12:54595663..54596788hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036880
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610613
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