A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592458



Internal ID20965529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11934638..13951892hg38UCSC Ensembl
chr10:11976637..13993892hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382017255
hg192017256
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217401
Samples
Known GenesBEND7, CAMK1D, CCDC3, CDC123, DHTKD1, FRMD4A, LOC283070, MCM10, MIR4480, NUDT5, OPTN, PHYH, PRPF18, SEC61A2, SEPHS1, UCMA, UPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592458
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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