A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179711



Internal ID20746751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28764403..28766418hg38UCSC Ensembl
chr17:27091421..27093436hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382016
hg192016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513167
Supporting Variants
Samples
Known GenesFAM222B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179711
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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