A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634861



Internal ID21583166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182156683..182156683hg38UCSC Ensembl
chr4:183077836..183077836hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124554
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634861
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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