A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001444



Internal ID16947710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:115100154..115146253hg38UCSC Ensembl
Outerchr3:114819001..114865100hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3846100
hg1946100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955327
Supporting Variants
SamplesBILGI_BIOE
Known GenesZBTB20
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001444
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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