A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526216



Internal ID21850574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170546743..170546873hg38UCSC Ensembl
chr1:170515884..170516014hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981943
Supporting Variants
Samples
Known GenesGORAB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526216
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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