A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392785



Internal ID22450655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15980020..15985287hg38UCSC Ensembl
chr21:17352340..17357607hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg385268
hg195268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962712
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392785
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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