A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5407876



Internal ID187206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150842340..150842391hg38UCSC Ensembl
chr6:151163476..151163527hg19UCSC Ensembl
Cytoband6q25.1
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 Variantsnssv16989975
Samples
Known GenesPLEKHG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5407876
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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