A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970554



Internal ID22745489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65123228..65123228hg38UCSC Ensembl
chr17:63119346..63119346hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970554
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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