A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561881



Internal ID20934952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87912735..88136103hg38UCSC Ensembl
chr9:90527650..90751018hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38223369
hg19223369
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281334
Samples
Known GenesCDK20, SPATA31C1, SPATA31C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561881
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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