A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001853



Internal ID19194023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39872159..39890960hg38UCSC Ensembl
Outerchr19:40362799..40381600hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3818802
hg1918802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150919
Supporting Variants
SamplesKWB1
Known GenesFCGBP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001853
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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