A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469459



Internal ID22527349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14867730..14868754hg38UCSC Ensembl
chr10:14909729..14910753hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381025
hg191025
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863451
Supporting Variants
Samples
Known GenesHSPA14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469459
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