A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151847



Internal ID19196945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:15186392..15192893hg38UCSC Ensembl
Outerchr3:15227899..15234400hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386502
hg196502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999030
SamplesKWB1
Known GenesCOL6A4P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151847
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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