A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504413



Internal ID281217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3925662..3949739hg38UCSC Ensembl
chr11:3946892..3970969hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824078
hg1924078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041570
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504413
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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