A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444790



Internal ID21102343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127310012..127310582hg38UCSC Ensembl
chr9:130072291..130072861hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223219
Samples
Known GenesGARNL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444790
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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