A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560987



Internal ID21885342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178900466..178900561hg38UCSC Ensembl
chr5:178327467..178327562hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014277
Supporting Variants
Samples
Known GenesZFP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560987
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