A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275059



Internal ID20484277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112373687..112409477hg38UCSC Ensembl
chr6:112694889..112730679hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3835791
hg1935791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733817
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275059
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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