A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638982



Internal ID21587287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10201602..10201602hg38UCSC Ensembl
chr5:10201714..10201714hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130622
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638982
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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