A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545573



Internal ID20918804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16746915..21192302hg38UCSC Ensembl
chr3:16788422..21233794hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384445388
hg194445373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261142
Samples
Known GenesEFHB, KAT2B, KCNH8, LOC339862, MIR3714, MIR4791, PLCL2, PP2D1, RAB5A, SATB1, SGOL1, SGOL1-AS1, TBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545573
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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