A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618037



Internal ID21566342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175282560..175282560hg38UCSC Ensembl
chr1:175251696..175251696hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061635
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618037
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