A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211423



Internal ID20778463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15110376..15205291hg38UCSC Ensembl
chr3:15151883..15246798hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3894916
hg1994916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359383
Supporting Variants
Samples
Known GenesCOL6A4P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211423
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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