A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429609



Internal ID21087162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4489802..4613482hg38UCSC Ensembl
chr9:4489802..4613482hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38123681
hg19123681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191159
Samples
Known GenesSLC1A1, SPATA6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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