A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560005



Internal ID20933076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81726183..81726617hg38UCSC Ensembl
chr9:84341098..84341532hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281167
Samples
Known GenesLOC101927502
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560005
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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