A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118618



Internal ID19275653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39882960..39895060hg38UCSC Ensembl
Outerchr19:40373600..40385700hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3812101
hg1912101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959132
SamplesKWS1
Known GenesFCGBP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118618
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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