A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583297



Internal ID21531820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:137911409..137911647hg38UCSC Ensembl
chr2:138668979..138669217hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109256
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583297
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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