A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368881



Internal ID22594550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11481478..11481478hg38UCSC Ensembl
chr12:11634412..11634412hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368881
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer