A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573426



Internal ID21521831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170046790..170046915hg38UCSC Ensembl
chr4:170967941..170968066hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129134
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573426
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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