A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459644



Internal ID21117197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116796501..116801800hg38UCSC Ensembl
chr11:116667217..116672516hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1320n223
Supporting Variantsnssv17987109
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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