A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955282



Internal ID17304155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:167836891..167843890hg38UCSC Ensembl
Outerchr2:168693401..168700400hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003063
SamplesBILGI_BIOE
Known GenesB3GALT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955282
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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