A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105993



Internal ID21467310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5043203..5043279hg38UCSC Ensembl
chr19:5043214..5043290hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590998
Supporting Variants
SamplesHG03065
Known GenesKDM4B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105993
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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