A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179417



Internal ID20746457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62068501..62073600hg38UCSC Ensembl
chr15:62360700..62365799hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514405
Supporting Variants
Samples
Known GenesC2CD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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