A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561837



Internal ID20934908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91350638..91351239hg38UCSC Ensembl
chr9:94112920..94113521hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281399
Samples
Known GenesAUH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561837
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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