A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284142



Internal ID20493360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17376513..17381043hg38UCSC Ensembl
chr6:17376744..17381274hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384531
hg194531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737916
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284142
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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