A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285974



Internal ID20495192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89607764..89607897hg38UCSC Ensembl
chr6:90317483..90317616hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750275
Supporting Variants
Samples
Known GenesANKRD6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285974
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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