A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445213



Internal ID21102766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16233247..16556728hg38UCSC Ensembl
chr11:16254793..16578275hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38323482
hg19323483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988457
Samples
Known GenesSOX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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