A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636155



Internal ID21584460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174911581..174911581hg38UCSC Ensembl
chr4:175832732..175832732hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120699
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636155
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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