A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752226



Internal ID21386213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79671139..79673138hg38UCSC Ensembl
chr17:77645001..77647000hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432610
Supporting Variants
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752226
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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