A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122417



Internal ID21419471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72045467..72045467hg38UCSC Ensembl
chr3:72094618..72094618hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605377
Supporting Variants
SamplesHG00731
Known GenesLINC00877
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122417
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