A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267596



Internal ID20476814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11514163..11514163hg38UCSC Ensembl
chr10:11556162..11556162hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763659
Supporting Variants
Samples
Known GenesUSP6NL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267596
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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