A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436494



Internal ID21094047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3864308..3870079hg38UCSC Ensembl
chr11:3885538..3891309hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385772
hg195772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990683
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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