A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532364



Internal ID21856720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:76183779..76183896hg38UCSC Ensembl
chr1:76649464..76649581hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984831
Supporting Variants
Samples
Known GenesST6GALNAC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532364
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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