A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622213



Internal ID21570518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33863704..33863704hg38UCSC Ensembl
chr4:33865326..33865326hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg388568
hg198568
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119677
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622213
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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