A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456569



Internal ID22514447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102855181..102871240hg38UCSC Ensembl
chr10:104614938..104630997hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3816060
hg1916060
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848261
Supporting Variants
Samples
Known GenesAS3MT, C10orf32, C10orf32-ASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456569
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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