A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636114



Internal ID21584419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165069827..165069827hg38UCSC Ensembl
chr4:165990979..165990979hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126121
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636114
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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