A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910104



Internal ID22685314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102852051..102871611hg38UCSC Ensembl
chr10:104611808..104631368hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3819561
hg1919561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362092
Samples
Known GenesAS3MT, C10orf32, C10orf32-ASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910104
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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