A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960434



Internal ID22735407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35227619..35227619hg38UCSC Ensembl
chr6:35195396..35195396hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438579
Samples
Known GenesSCUBE3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960434
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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