A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179603



Internal ID20746643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27637677..27745650hg38UCSC Ensembl
chr17:25964703..26072676hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38107974
hg19107974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506670
Supporting Variants
Samples
Known GenesLGALS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179603
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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