A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582616



Internal ID21531130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206105805..206106352hg38UCSC Ensembl
chr2:206970529..206971076hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109983
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582616
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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