A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541816



Internal ID20915084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154298754..154300335hg38UCSC Ensembl
chr1:154271230..154272811hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381582
hg191582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541816
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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