A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462010



Internal ID22519895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91148048..91151784hg38UCSC Ensembl
chr12:91541825..91545561hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg383737
hg193737
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851708
Supporting Variants
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462010
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