A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705289



Internal ID21377565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13338728..13338777hg38UCSC Ensembl
chr12:13491662..13491711hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390138
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705289
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0172414


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