A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071925



Internal ID20638965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32167808..32168321hg38UCSC Ensembl
chr21:33540120..33540633hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550179
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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