A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572710



Internal ID20945781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97995701..97996744hg38UCSC Ensembl
chr9:100757983..100759026hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381044
hg191044
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281596
Samples
Known GenesANP32B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572710
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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