A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919039



Internal ID22694261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71984316..71984631hg38UCSC Ensembl
chr11:71695362..71695677hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364449
Samples
Known GenesRNF121
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919039
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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