A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276561



Internal ID20843601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75754131..76110069hg38UCSC Ensembl
chr7:75383449..75739387hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38355939
hg19355939
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575018
Supporting Variants
Samples
Known GenesCCL24, CCL26, MDH2, MIR4651, POR, RHBDD2, SNORA14A, STYXL1, TMEM120A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276561
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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