A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102902



Internal ID20669942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57560901..57562800hg38UCSC Ensembl
chr3:57546628..57548527hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366726
Supporting Variants
Samples
Known GenesPDE12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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