A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634497



Internal ID21582802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104941463..104941463hg38UCSC Ensembl
chr6:105389338..105389338hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156545
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634497
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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