A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469726



Internal ID21127279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66137704..66140906hg38UCSC Ensembl
chr11:65905175..65908377hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383203
hg193203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992544
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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