A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577837



Internal ID20950908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2777652..5831302hg38UCSC Ensembl
chr10:2819844..5873265hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383053651
hg193053422
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225743
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3, AKR1C4, AKR1C6P, AKR1CL1, AKR1E2, ASB13, CALML3, CALML5, FAM208B, GDI2, KLF6, LINC00702, LINC00703, LINC00704, LINC00705, MIR6078, NET1, PFKP, PITRM1, PITRM1-AS1, TUBAL3, UCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577837
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer