A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576097



Internal ID21524531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201683071..201683148hg38UCSC Ensembl
chr2:202547794..202547871hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111393
SamplesNA19238
Known GenesMPP4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576097
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