A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911035



Internal ID22686247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4037447..4037549hg38UCSC Ensembl
chr11:4058677..4058779hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351500
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911035
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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