A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526780



Internal ID21851138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:186271574..186276114hg38UCSC Ensembl
chr1:186240706..186245246hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg384541
hg194541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982114
Supporting Variants
Samples
Known GenesMIR548F1, RNU6-72P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526780
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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