A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146403



Internal ID19201914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:37128200..37128266hg38UCSC Ensembl
Outerchr1:37593801..37593867hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999609
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146403
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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