A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563965



Internal ID20937036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128398538..128399104hg38UCSC Ensembl
chr9:131160817..131161383hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563965
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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