A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460754



Internal ID21118307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96584005..96589706hg38UCSC Ensembl
chr11:96455004..96460706hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385702
hg195703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460754
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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