A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126220



Internal ID21509654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16538202..16538202hg38UCSC Ensembl
chr3:16579709..16579709hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608299
Supporting Variants
SamplesNA20847
Known GenesLINC00690
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126220
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