A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573359



Internal ID21521763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:134036475..134047114hg38UCSC Ensembl
chr2:134794046..134804685hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3810640
hg1910640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17108693
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573359
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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