A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569929



Internal ID20943000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109177635..109178530hg38UCSC Ensembl
chr9:111939915..111940810hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279493
Samples
Known GenesEPB41L4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569929
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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