A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531108



Internal ID21855464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240780820..240781918hg38UCSC Ensembl
chr1:240944120..240945218hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5983128
Supporting Variants
Samples
Known GenesRGS7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531108
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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