A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190798



Internal ID20757838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13525878..13526462hg38UCSC Ensembl
chr12:13678812..13679396hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190798
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01771


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