A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261441



Internal ID20470659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84701335..84701388hg38UCSC Ensembl
chr6:85411053..85411106hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739616
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261441
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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