A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468882



Internal ID21126435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63604643..63608053hg38UCSC Ensembl
chr11:63372115..63375525hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg383411
hg193411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993800
Samples
Known GenesPLA2G16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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