A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907837



Internal ID22683047
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 StatusM
Merged Variants
Supporting Variantsnssv17365793
Samples
Known GenesDIP2C, PRR26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907837
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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