A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485649



Internal ID22543560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148058633..148061934hg38UCSC Ensembl
chr3:147776420..147779721hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg383302
hg193302
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485649
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