A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546802



Internal ID20920012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82431283..82432649hg38UCSC Ensembl
chr1:82896966..82898332hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381367
hg191367
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546802
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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