A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283467



Internal ID20492685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88283108..88283166hg38UCSC Ensembl
chr6:88992827..88992885hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733757
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283467
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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