A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734835



Internal ID20510774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158659589..158659919hg38UCSC Ensembl
chr1:158629379..158629709hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285077
Samples
Known GenesSPTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734835
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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