A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637082



Internal ID21585387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6360916..6360916hg38UCSC Ensembl
chr5:6361029..6361029hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150134
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637082
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