A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288389



Internal ID20497607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101366800..101366800hg38UCSC Ensembl
chr10:103126557..103126557hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767611
Supporting Variants
Samples
Known GenesBTRC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288389
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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