A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752465



Internal ID21386182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12261684..12262683hg38UCSC Ensembl
chr17:12165001..12166000hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432442
Supporting Variants
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752465
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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