A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562750



Internal ID20935821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100155064..100155624hg38UCSC Ensembl
chr9:102917346..102917906hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279298
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562750
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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