A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624384



Internal ID21572689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8501386..8501386hg38UCSC Ensembl
chr1:8561446..8561446hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066507
SamplesNA20509
Known GenesRERE
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624384
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