A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489836



Internal ID22547757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192844899..192884515hg38UCSC Ensembl
chr3:192562688..192602304hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3839617
hg1939617
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835780
Supporting Variants
Samples
Known GenesMB21D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489836
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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