A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535106



Internal ID310813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107722172..107722189hg38UCSC Ensembl
chr6:108043376..108043393hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987908
Samples
Known GenesSCML4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535106
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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