A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455565



Internal ID21113118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133398533..133445103hg38UCSC Ensembl
chr9:136263660..136310224hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3846571
hg1946565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235417
Samples
Known GenesADAMTS13, C9orf96, REXO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455565
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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