A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467992



Internal ID21125545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99223091..99226796hg38UCSC Ensembl
chr11:99093822..99097527hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383706
hg193706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996526
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467992
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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