A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574882



Internal ID20947953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13282922..13283127hg38UCSC Ensembl
chr6:13283154..13283359hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271900
Samples
Known GenesLOC100130357, PHACTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574882
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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