A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953868



Internal ID17302742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:26936175..26962474hg38UCSC Ensembl
Outerchr17:25263201..25289500hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3826300
hg1926300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000289
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953868
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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