A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828508



Internal ID22603443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163232183..163236190hg38UCSC Ensembl
chr1:163201973..163205980hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg384008
hg194008
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461965
Samples
Known GenesRGS5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828508
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