A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192255



Internal ID20759295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5244957..5246217hg38UCSC Ensembl
chr12:5354123..5355383hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg381261
hg191261
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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