A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917187



Internal ID22692406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7510137..7510225hg38UCSC Ensembl
chr11:7531368..7531456hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359125
Samples
Known GenesOLFML1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917187
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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