A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609324



Internal ID20982395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154462267..154463035hg38UCSC Ensembl
chr6:154783401..154784169hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216664
Samples
Known GenesCNKSR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609324
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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