A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276026



Internal ID20485244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78115617..78115679hg38UCSC Ensembl
chr17:76111698..76111760hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746699
Supporting Variants
Samples
Known GenesTMC6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276026
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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