A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190659



Internal ID20757699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14018401..14025700hg38UCSC Ensembl
chr17:13921718..13929017hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504036
Supporting Variants
Samples
Known GenesCDRT15P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190659
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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