A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465192



Internal ID21122745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44721021..44725741hg38UCSC Ensembl
chr11:44742571..44747291hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg384721
hg194721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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