A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546573



Internal ID20919783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96114819..96116670hg38UCSC Ensembl
chr1:96580375..96582226hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381852
hg191852
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546573
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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