A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628419



Internal ID21576724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90367846..90367846hg38UCSC Ensembl
chr6:91077565..91077565hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139716
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628419
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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