A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350098



Internal ID22575767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4205328..4205432hg38UCSC Ensembl
chr12:4314494..4314598hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919643
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350098
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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