A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544588



Internal ID20917826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108867933..109235536hg38UCSC Ensembl
chr1:109410555..109778158hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38367604
hg19367604
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247274
Samples
Known GenesC1orf194, CLCC1, GPSM2, KIAA1324, SARS, SCARNA2, TAF13, TMEM167B, WDR47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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