A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742189



Internal ID20518169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14792449..14792569hg38UCSC Ensembl
chr12:14945383..14945503hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274127
Samples
Known GenesWBP11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742189
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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