A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452504



Internal ID21110057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30032339..30034286hg38UCSC Ensembl
chr11:30053886..30055833hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381948
hg191948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452504
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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