A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460108



Internal ID22517994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179733788..179748632hg38UCSC Ensembl
chr1:179702923..179717767hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3814845
hg1914845
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828434
Supporting Variants
Samples
Known GenesFAM163A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460108
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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