A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268576



Internal ID20477794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66400502..66400502hg38UCSC Ensembl
chr1:66866185..66866185hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753012
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268576
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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