A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573445



Internal ID21521850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170237234..170454415hg38UCSC Ensembl
chr4:171158385..171375566hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38217182
hg19217182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126710
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573445
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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