A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548994



Internal ID20922172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196914542..196914956hg38UCSC Ensembl
chr2:197779266..197779680hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257074
Samples
Known GenesPGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548994
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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