A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936175



Internal ID22711526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38822321..38823414hg38UCSC Ensembl
chr17:36978574..36979667hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381094
hg191094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387230
Samples
Known GenesCWC25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936175
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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