A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913788



Internal ID22689004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49198159..49199513hg38UCSC Ensembl
chr11:49219711..49221065hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367984
Samples
Known GenesFOLH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913788
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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