A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488880



Internal ID22546798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39103575..39107746hg38UCSC Ensembl
chr21:40475501..40479672hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg384172
hg194172
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871081
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488880
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