A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292839



Internal ID20502057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122644023..122644023hg38UCSC Ensembl
chr10:124403539..124403539hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292839
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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