A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525485



Internal ID21849843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109541365..109541365hg38UCSC Ensembl
chr1:110083987..110083987hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054549
Supporting Variants
Samples
Known GenesGPR61
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525485
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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