A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560068



Internal ID20933139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117837743..117838546hg38UCSC Ensembl
chr9:120600021..120600824hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7926n223
Supporting Variantsnssv18279705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560068
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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