A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576184



Internal ID21524620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4420271..4420334hg38UCSC Ensembl
chr1:4480331..4480394hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065791
SamplesHG00732
Known GenesLOC284661
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576184
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer