A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469900



Internal ID21127453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102630301..102636200hg38UCSC Ensembl
chr11:102501032..102506931hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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