A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001686



Internal ID17294638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:11029275..11038374hg38UCSC Ensembl
Outerchr2:11169401..11178500hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953447
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001686
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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