A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585917



Internal ID21777960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119912780..119913634hg38UCSC Ensembl
chr10:121672292..121673146hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017802
Supporting Variants
Samples
Known GenesSEC23IP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585917
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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