A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568373



Internal ID21516720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43522349..43522426hg38UCSC Ensembl
chr5:43522451..43522528hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138170
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568373
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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