A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968446



Internal ID22743381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40118752..40118752hg38UCSC Ensembl
chr17:38275005..38275005hg19UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968446
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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