A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639350



Internal ID21587655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24029451..24029451hg38UCSC Ensembl
chr6:24029679..24029679hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144909
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639350
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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