A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409659



Internal ID188979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88904861..88904912hg38UCSC Ensembl
chr10:90664618..90664669hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036374
Samples
Known GenesSTAMBPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409659
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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