A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453168



Internal ID21110721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99954579..99955014hg38UCSC Ensembl
chr9:102716861..102717296hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187532
Samples
Known GenesSTX17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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