A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260708



Internal ID20469926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234669939..234669939hg38UCSC Ensembl
chr1:234805685..234805685hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260708
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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