A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145825



Internal ID18854754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:426999..434600hg38UCSC Ensembl
Outerchr19:426999..434600hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387602
hg197602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997185
SamplesKWB1
Known GenesSHC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1145825
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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