A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177476



Internal ID20744516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:831867..842879hg38UCSC Ensembl
chr17:735107..746119hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3811013
hg1911013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501793
Supporting Variants
Samples
Known GenesNXN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177476
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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