A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582914



Internal ID21531431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239938925..239938990hg38UCSC Ensembl
chr2:240878342..240878407hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17112437
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582914
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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