A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927955



Internal ID22703188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70028875..70029182hg38UCSC Ensembl
chr17:68025016..68025323hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377681
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927955
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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