A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924972



Internal ID22700199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32211766..32211837hg38UCSC Ensembl
chr11:32233312..32233383hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924972
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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