A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416214



Internal ID22474084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194382011..194382213hg38UCSC Ensembl
chr3:194102740..194102942hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416214
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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