A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539373



Internal ID20912671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106538333..106538906hg38UCSC Ensembl
chr1:107080955..107081528hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539373
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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