A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965454



Internal ID22740389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35226480..35226480hg38UCSC Ensembl
chr6:35194257..35194257hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440689
Samples
Known GenesSCUBE3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965454
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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