A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952641



Internal ID16954828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:204396873..204410972hg38UCSC Ensembl
Outerchr1:204366001..204380100hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3814100
hg1914100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999217
SamplesBILGI_BIOE
Known GenesPPP1R15B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952641
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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