A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951403



Internal ID17300277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:115098480..115109079hg38UCSC Ensembl
Outerchr1:115641101..115651700hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3810600
hg1910600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997207
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951403
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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