A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409938



Internal ID189258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101939624..101939675hg38UCSC Ensembl
chr10:103699381..103699432hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039873
Samples
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409938
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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