A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455143



Internal ID21112696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127701636..127707698hg38UCSC Ensembl
chr9:130463915..130469977hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386063
hg196063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226622
Samples
Known GenesC9orf117
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455143
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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