A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374161



Internal ID22599830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36188759..36188759hg38UCSC Ensembl
chr18:33768722..33768722hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970574
Supporting Variants
Samples
Known GenesMOCOS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374161
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