A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576217



Internal ID21524653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18714325..18714633hg38UCSC Ensembl
chr3:18755817..18756125hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123470
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576217
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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