A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098457



Internal ID20665497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182642447..182645634hg38UCSC Ensembl
chr3:182360235..182363422hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg383188
hg193188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372406
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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