A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558957



Internal ID20932028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13685478..13686354hg38UCSC Ensembl
chr6:13685710..13686586hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272410
Samples
Known GenesRANBP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558957
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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