A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485698



Internal ID22543609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151777049..151778998hg38UCSC Ensembl
chr3:151494837..151496786hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381950
hg191950
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834369
Supporting Variants
Samples
Known GenesLOC201651, MIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485698
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