A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070867



Internal ID20637907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16334598..16344782hg38UCSC Ensembl
chr21:17706919..17717103hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3810185
hg1910185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551705
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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