A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469606



Internal ID22527496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133558664..133569071hg38UCSC Ensembl
chr10:135372168..135382575hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3810408
hg1910408
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849148
Supporting Variants
Samples
Known GenesSPRNP1, SYCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469606
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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