A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189105



Internal ID20756145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107760401..107762000hg38UCSC Ensembl
chr12:108154178..108155777hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465072
Supporting Variants
Samples
Known GenesPRDM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189105
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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