A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269533



Internal ID20478751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28117264..28117376hg38UCSC Ensembl
chr6:28085042..28085154hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733783
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269533
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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