A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565843



Internal ID20938914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104913798..104914520hg38UCSC Ensembl
chr9:107676079..107676801hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279372
Samples
Known GenesABCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565843
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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