A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451102



Internal ID21108655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112866561..112867209hg38UCSC Ensembl
chr9:115628841..115629489hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229765
Samples
Known GenesSNX30
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451102
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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