A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581648



Internal ID21530150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55132387..55132720hg38UCSC Ensembl
chr4:55998554..55998887hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131891
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581648
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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