A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449163



Internal ID21106716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91869996..92164079hg38UCSC Ensembl
chr9:94632278..94926361hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38294084
hg19294084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236948
Samples
Known GenesLINC00475, LOC100128076, ROR2, SPTLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449163
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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