A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390458



Internal ID21381593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112100161..112100229hg38UCSC Ensembl
chr12:112537965..112538033hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705467
Samples
Known GenesNAA25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390458
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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