A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418904



Internal ID21076457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124854801..124959700hg38UCSC Ensembl
chr8:125867043..125971942hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38104900
hg19104900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235128
Samples
Known GenesLINC00964
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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