A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973155



Internal ID22748090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125919195..125919195hg38UCSC Ensembl
chr10:127607764..127607764hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354316
Samples
Known GenesFANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973155
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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