A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462169



Internal ID22520054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84350084..84355569hg38UCSC Ensembl
chr10:86109840..86115325hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg385486
hg195486
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859996
Supporting Variants
Samples
Known GenesCCSER2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462169
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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