A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367343



Internal ID22593012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53470127..53471321hg38UCSC Ensembl
chr12:53863911..53865105hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381195
hg191195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938148
Supporting Variants
Samples
Known GenesPCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367343
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer