A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584945



Internal ID20958016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29510330..30674089hg38UCSC Ensembl
chr10:29799259..30963018hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381163760
hg191163760
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n223
Supporting Variantsnssv18224902
Samples
Known GenesKIAA1462, LYZL2, MAP3K8, MIR604, MIR7162, MIR938, MTPAP, SVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584945
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