A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630841



Internal ID21579146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2504580..2504580hg38UCSC Ensembl
chr6:2504814..2504814hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148084
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630841
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