A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628616



Internal ID21576921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170079620..170079620hg38UCSC Ensembl
chr6:170394844..170394844hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153909
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628616
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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