A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924524



Internal ID22699751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118239575..118241480hg38UCSC Ensembl
chr11:118110290..118112195hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381906
hg191906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365342
Samples
Known GenesMPZL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924524
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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