A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460054



Internal ID22517940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102863977..102865984hg38UCSC Ensembl
chr10:104623734..104625741hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg382008
hg192008
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856842
Supporting Variants
Samples
Known GenesC10orf32, C10orf32-ASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460054
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer