A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574394



Internal ID20947465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120835447..120836532hg38UCSC Ensembl
chr9:123597725..123598810hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279742
Samples
Known GenesPSMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574394
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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