A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443584



Internal ID21101137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16370079..16370486hg38UCSC Ensembl
chr11:16391625..16392032hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988486
Samples
Known GenesSOX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443584
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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