A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564174



Internal ID20937245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125155601..125156602hg38UCSC Ensembl
chr9:127917880..127918881hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279865
Samples
Known GenesPPP6C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564174
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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