A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099499



Internal ID20666539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186106391..186106855hg38UCSC Ensembl
chr3:185824180..185824644hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357634
Supporting Variants
Samples
Known GenesETV5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099499
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