A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281787



Internal ID20491005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178900520..178900520hg38UCSC Ensembl
chr5:178327521..178327521hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753717
Supporting Variants
Samples
Known GenesZFP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281787
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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