A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456428



Internal ID22514306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3452300..3457959hg38UCSC Ensembl
chr12:3561466..3567125hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg385660
hg195660
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866195
Supporting Variants
Samples
Known GenesPRMT8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456428
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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