A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455503



Internal ID21113056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124441980..124484258hg38UCSC Ensembl
chr9:127204259..127246537hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3842279
hg1942279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228298
Samples
Known GenesNR5A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455503
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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