A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557715



Internal ID20930786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75901418..82872806hg38UCSC Ensembl
chr9:78516334..85487721hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg386971389
hg196971388
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281004
Samples
Known GenesCEP78, FOXB2, GCNT1, GNA14, GNAQ, LOC101927450, LOC101927502, PCA3, PCSK5, PRUNE2, PSAT1, RFK, RPSAP9, SPATA31D1, SPATA31D3, SPATA31D4, SPATA31D5P, TLE1, TLE4, VPS13A, VPS13A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557715
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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