A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566594



Internal ID20939665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4979239..5734870hg38UCSC Ensembl
chr7:5018870..5774501hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38755632
hg19755632
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6546n223
Supporting Variantsnssv18274547
Samples
Known GenesACTB, FBXL18, FSCN1, MIR589, MIR6874, RBAK, RBAKDN, RBAK-RBAKDN, RNF216, RNF216-IT1, RNF216P1, SLC29A4, TNRC18, WIPI2, ZNF890P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566594
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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