A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909838



Internal ID22685048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:24578363..24578416hg38UCSC Ensembl
chr12:24731297..24731350hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367576
Samples
Known GenesLINC00477
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909838
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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