A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952353



Internal ID17301227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:62880140..62896139hg38UCSC Ensembl
Outerchr17:60957501..60973500hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3816000
hg1916000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998786
SamplesBILGI_BIOE
Known GenesMIR548W
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952353
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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