A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187483



Internal ID20754523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72269342..72278534hg38UCSC Ensembl
chr15:72561683..72570875hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg389193
hg199193
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503370
Supporting Variants
Samples
Known GenesPARP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187483
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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