A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548771



Internal ID20921953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222209701..222210997hg38UCSC Ensembl
chr2:223074420..223075716hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg381297
hg191297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259402
Samples
Known GenesPAX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548771
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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