A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539488



Internal ID20912783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207985950..207986668hg38UCSC Ensembl
chr2:208850674..208851392hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258575
Samples
Known GenesPLEKHM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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