A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188799



Internal ID20755839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28576780..28577460hg38UCSC Ensembl
chr17:26903798..26904478hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38681
hg19681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513273
Supporting Variants
Samples
Known GenesALDOC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188799
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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