A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632649



Internal ID21580954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1984701..1984701hg38UCSC Ensembl
chr5:1984815..1984815hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136498
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632649
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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