A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546683



Internal ID20919893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100583728..100587011hg38UCSC Ensembl
chr1:101049284..101052567hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg383284
hg193284
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546683
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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