A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575890



Internal ID21524323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20512645..20513260hg38UCSC Ensembl
chr2:20712405..20713020hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109958
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575890
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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