A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581168



Internal ID20954239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129841859..129844086hg38UCSC Ensembl
chr10:131640123..131642350hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382228
hg192228
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232378
Samples
Known GenesEBF3, MIR4297
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581168
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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