A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952361



Internal ID16954548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:65009183..65052982hg38UCSC Ensembl
Outerchr17:63005301..63049100hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3843800
hg1943800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998794
SamplesBILGI_BIOE
Known GenesGNA13
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952361
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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