A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561366



Internal ID20934437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105332130..105529172hg38UCSC Ensembl
chr7:104972577..105169619hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38197043
hg19197043
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272241
Samples
Known GenesPUS7, SRPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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