A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545194



Internal ID20918427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87509108..87510219hg38UCSC Ensembl
chr1:87974791..87975902hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381112
hg191112
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545194
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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