A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353584



Internal ID22579253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:33150738..33194780hg38UCSC Ensembl
chr12:33303672..33347715hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3844043
hg1944044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353584
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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