A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450351



Internal ID22508221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68812217..68814417hg38UCSC Ensembl
chr10:70571974..70574174hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450351
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