A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451974



Internal ID21109527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30549427..30549963hg38UCSC Ensembl
chr11:30570974..30571510hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990340
Samples
Known GenesMPPED2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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