A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638172



Internal ID21586477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166021091..166021091hg38UCSC Ensembl
chr6:166434579..166434579hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157786
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638172
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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