A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628371



Internal ID21576676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126064642..126064642hg38UCSC Ensembl
chr6:126385788..126385788hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141691
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628371
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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