A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153846



Internal ID19203201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:90326237..90388938hg38UCSC Ensembl
Outerchr2:90385099..90447800hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3862702
hg1962702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002501
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153846
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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