A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563516



Internal ID20936587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72601586..72602465hg38UCSC Ensembl
chr9:75216502..75217381hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7829n223
Supporting Variantsnssv18280937
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563516
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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