A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536232



Internal ID20909585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84485009..84486320hg38UCSC Ensembl
chr1:84950692..84952003hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253915
Samples
Known GenesRPF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536232
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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