A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979386



Internal ID22754321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65037777..65037777hg38UCSC Ensembl
chr17:63033895..63033895hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379006
Samples
Known GenesGNA13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979386
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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