A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086846



Internal ID21434249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34506225..34506225hg38UCSC Ensembl
chr13:35080362..35080362hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659199
Supporting Variants
SamplesHG00731
Known GenesLINC00457
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086846
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