A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563903



Internal ID20936974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97663586..97664133hg38UCSC Ensembl
chr9:100425868..100426415hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281584
Samples
Known GenesNCBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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