A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409484



Internal ID188805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107814966..107814966hg38UCSC Ensembl
chr6:108136170..108136170hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987919
Samples
Known GenesSCML4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409484
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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