A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431674



Internal ID21089227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29236230..29317409hg38UCSC Ensembl
chr9:29236228..29317407hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3881180
hg1981180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431674
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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