A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274550



Internal ID20841590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4983650..5730763hg38UCSC Ensembl
chr7:5023281..5770394hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38747114
hg19747114
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559174
Supporting Variants
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)nssv18274550
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0005


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