A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556566



Internal ID20929637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113002872..113120855hg38UCSC Ensembl
chr9:115765152..115883135hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38117984
hg19117984
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279629
Samples
Known GenesFAM225A, FAM225B, ZFP37, ZNF883
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556566
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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