A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711989



Internal ID135655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19026030..19237111hg38UCSC Ensembl
chr17:18929343..19140424hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38211082
hg19211082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146200
Supporting Variants
Samples
Known GenesGRAP, GRAPL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711989
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.145722


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