A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564558



Internal ID20937629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105545205..105764347hg38UCSC Ensembl
chr9:108307486..108526628hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38219143
hg19219143
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279401
Samples
Known GenesFKTN, FSD1L, TAL2, TMEM38B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564558
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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