A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267635



Internal ID20476853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27473914..27474124hg38UCSC Ensembl
chr6:27441693..27441903hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267635
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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