A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573408



Internal ID20946479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125229137..125230227hg38UCSC Ensembl
chr9:127991416..127992506hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279877
Samples
Known GenesRABEPK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573408
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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