A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998832



Internal ID17291784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:83229132..83243831hg38UCSC Ensembl
Outerchr17:81176901..81191600hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3814700
hg1914700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952399
Supporting Variants
SamplesBILGI_BIOE
Known GenesFLJ43681
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998832
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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