A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424209



Internal ID21081762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22411286..22673187hg38UCSC Ensembl
chr9:22411285..22673186hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38261902
hg19261902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217925
Samples
Known GenesDMRTA1, FLJ35282
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424209
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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