A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956103



Internal ID22731295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118297626..118297626hg38UCSC Ensembl
chr6:118618789..118618789hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420270
Samples
Known GenesSLC35F1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956103
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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