A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919534



Internal ID22694756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47384111..47384867hg38UCSC Ensembl
chr11:47405662..47406418hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919534
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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