A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274406



Internal ID20483624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77335712..77335769hg38UCSC Ensembl
chr17:75331794..75331851hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731663
Supporting Variants
Samples
Known GenesSEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274406
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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