A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258959



Internal ID20468147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168119213..168119213hg38UCSC Ensembl
chr1:168088451..168088451hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764020
Supporting Variants
Samples
Known GenesGPR161
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16258959
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