A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100496



Internal ID20667536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186210539..186211168hg38UCSC Ensembl
chr3:185928328..185928957hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356377
Supporting Variants
Samples
Known GenesDGKG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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