A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455263



Internal ID21112816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135873876..135874239hg38UCSC Ensembl
chr9:138765722..138766085hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234718
Samples
Known GenesCAMSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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