A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363776



Internal ID22589445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3761779..3768163hg38UCSC Ensembl
chr12:3870945..3877329hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg386385
hg196385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363776
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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