A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582945



Internal ID21531463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238965057..238965178hg38UCSC Ensembl
chr2:239886753..239886874hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17112387
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582945
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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