A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495092



Internal ID272215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4079251..4079532hg38UCSC Ensembl
chr11:4100481..4100762hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041579
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495092
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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