A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428270



Internal ID21085823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26183340..26853973hg38UCSC Ensembl
chr9:26183338..26853971hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38670634
hg19670634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228794
Samples
Known GenesCAAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428270
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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