A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267193



Internal ID20476411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158892892..158897617hg38UCSC Ensembl
chr6:159313924..159318649hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384726
hg194726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730752
Supporting Variants
Samples
Known GenesC6orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267193
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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