A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758083



Internal ID20533943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227494364..227506969hg38UCSC Ensembl
chr1:227682065..227694670hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3812606
hg1912606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758083
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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