A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542787



Internal ID20916039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200621575..200622132hg38UCSC Ensembl
chr1:200590703..200591260hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542787
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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