A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628480



Internal ID21576785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41749505..41749505hg38UCSC Ensembl
chr6:41717243..41717243hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159047
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628480
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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