A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467367



Internal ID21124920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36393238..36399572hg38UCSC Ensembl
chr11:36414788..36421122hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386335
hg196335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989916
Samples
Known GenesPRR5L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467367
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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