A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978987



Internal ID22753922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69915742..69915742hg38UCSC Ensembl
chr17:67911883..67911883hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978987
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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