A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911573



Internal ID22686788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4163840..4251032hg38UCSC Ensembl
chr11:4185070..4272262hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3887193
hg1987193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358362
Samples
Known GenesLOC100506082
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911573
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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