A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633598



Internal ID21581903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6932360..6932360hg38UCSC Ensembl
chr6:6932593..6932593hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159554
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633598
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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