A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633435



Internal ID21581740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132792352..132792352hg38UCSC Ensembl
chr6:133113491..133113491hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155580
SamplesHG03371
Known GenesSLC18B1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633435
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