A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540999



Internal ID20914284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162532225..162532879hg38UCSC Ensembl
chr1:162502015..162502669hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540999
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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