A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096409



Internal ID20663449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155255469..155382367hg38UCSC Ensembl
chr3:154973258..155100156hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38126899
hg19126899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372091
Supporting Variants
Samples
Known GenesLOC100507537
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096409
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