A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563397



Internal ID20936468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124665008..124666292hg38UCSC Ensembl
chr9:127427287..127428571hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381285
hg191285
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279835
Samples
Known GenesMIR181A2HG, NR6A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563397
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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