A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547602



Internal ID21871957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138765722..138770710hg38UCSC Ensembl
chr5:138101411..138106399hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg384989
hg194989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012917
Supporting Variants
Samples
Known GenesCTNNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547602
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