A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286379



Internal ID20495597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41109077..41109129hg38UCSC Ensembl
chr6:41076816..41076868hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746551
Supporting Variants
Samples
Known GenesADCY10P1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286379
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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