A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105281



Internal ID21498829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44645128..44645128hg38UCSC Ensembl
chr19:45148437..45148437hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660993
Supporting Variants
SamplesNA19239
Known GenesPVR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105281
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