A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594866



Internal ID21543466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95647108..95677060hg38UCSC Ensembl
chr10:97406865..97436817hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3829953
hg1929953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072050
SamplesHG02818
Known GenesALDH18A1, TCTN3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594866
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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