A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629001



Internal ID21577306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126222910..126222910hg38UCSC Ensembl
chr6:126544056..126544056hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153643
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629001
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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