A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080788



Internal ID21490219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51551608..51551608hg38UCSC Ensembl
chr15:51843805..51843805hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386080
hg196080
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657118
Supporting Variants
SamplesNA19238
Known GenesDMXL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080788
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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