A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556620



Internal ID20929691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116295316..116297028hg38UCSC Ensembl
chr9:119057595..119059307hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg381713
hg191713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279684
Samples
Known GenesPAPPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556620
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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