A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418494



Internal ID21076047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29139812..29161635hg38UCSC Ensembl
chr9:29139810..29161633hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3821824
hg1921824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179130
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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