A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186086



Internal ID20753126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38842711..38843605hg38UCSC Ensembl
chr17:36998964..36999858hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38895
hg19895
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186086
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00779


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