A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629036



Internal ID21577341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127720831..127720831hg38UCSC Ensembl
chr9:130483110..130483110hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159781
SamplesHG00731
Known GenesTTC16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629036
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