A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571827



Internal ID20944898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81641509..81704307hg38UCSC Ensembl
chr9:84256424..84319222hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3862799
hg1962799
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281158
Samples
Known GenesLOC101927502, TLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571827
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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