A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581830



Internal ID20954901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125086808..125095975hg38UCSC Ensembl
chr10:126775377..126784544hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg389168
hg199168
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235043
Samples
Known GenesCTBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581830
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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