A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455463



Internal ID21113016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129104785..129105085hg38UCSC Ensembl
chr9:131867064..131867364hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220978
Samples
Known GenesCRAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455463
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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