A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450012



Internal ID21107565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112609218..112871619hg38UCSC Ensembl
chr9:115371498..115633899hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38262402
hg19262402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227872
Samples
Known GenesINIP, KIAA1958, SNX30
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450012
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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