A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999129



Internal ID16945395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:197503471..197513670hg38UCSC Ensembl
Outerchr1:197472601..197482800hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3810200
hg1910200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952633
Supporting Variants
SamplesBILGI_BIOE
Known GenesDENND1B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999129
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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