A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449704



Internal ID22507574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102216936..102225732hg38UCSC Ensembl
chr12:102610714..102619510hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg388797
hg198797
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863619
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449704
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