A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5405389



Internal ID184733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100428644..100428695hg38UCSC Ensembl
chr6:100876520..100876571hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987017
Samples
Known GenesSIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5405389
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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