A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071808



Internal ID20638848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29252111..29254846hg38UCSC Ensembl
chr21:30624432..30627167hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg382736
hg192736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555239
Supporting Variants
Samples
Known GenesLINC00189
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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