A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394319



Internal ID22452189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32300591..32305523hg38UCSC Ensembl
chr21:33672902..33677834hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg384933
hg194933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964087
Supporting Variants
Samples
Known GenesMRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394319
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