A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579614



Internal ID21528095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143461905..143461964hg38UCSC Ensembl
chr5:142841470..142841529hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127588
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579614
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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