A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390519



Internal ID21381654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133194920..133195071hg38UCSC Ensembl
chr12:133771506..133771657hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705501
Samples
Known GenesZNF268
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390519
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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