A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752059



Internal ID21384535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158668247..158669098hg38UCSC Ensembl
chr1:158638037..158638888hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38852
hg19852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432970
Supporting Variants
SamplesBTQ016
Known GenesSPTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752059
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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