A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469198



Internal ID22527089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20873822..20875699hg38UCSC Ensembl
chr10:21162751..21164628hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851426
Supporting Variants
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469198
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