A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634255



Internal ID21582560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40694448..40694448hg38UCSC Ensembl
chr5:40694550..40694550hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122131
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634255
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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