A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889087



Internal ID22664099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50473259..50479959hg38UCSC Ensembl
chr6:50440972..50447672hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg386701
hg196701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889087
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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