A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194641



Internal ID20761681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13273985..13331650hg38UCSC Ensembl
chr17:13177302..13234967hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3857666
hg1957666
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194641
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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