A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456836



Internal ID21114389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96399901..96400100hg38UCSC Ensembl
chr11:96133065..96133264hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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