A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155374



Internal ID22085879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10322963..10330033hg38UCSC Ensembl
Outerchr17:10319903..10331274hg38UCSC Ensembl
Innerchr17:10226280..10233350hg19UCSC Ensembl
Outerchr17:10223220..10234591hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3811372
hg1911372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010083
Samples
Known GenesMYH13
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155374
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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