A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185164



Internal ID20752204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55306219..55474102hg38UCSC Ensembl
chr15:55598417..55766300hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38167884
hg19167884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515550
Supporting Variants
Samples
Known GenesC15orf65, CCPG1, DYX1C1, DYX1C1-CCPG1, MIR628, PIGB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185164
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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