A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428692



Internal ID21086245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29183795..29206854hg38UCSC Ensembl
chr9:29183793..29206852hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3823060
hg1923060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193581
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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