A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538180



Internal ID21862535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171844877..171970059hg38UCSC Ensembl
chr4:172766028..172891210hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38125183
hg19125183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996509
Supporting Variants
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538180
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