A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705467



Internal ID21377743
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 StatusS
Merged Variantsnsv4390458
Supporting Variants
Samples
Known GenesNAA25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705467
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0172414


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