A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365793



Internal ID22591462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:657552..658091hg38UCSC Ensembl
chr10:703492..704031hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907837
Supporting Variants
Samples
Known GenesDIP2C, PRR26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365793
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.16


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